Distal Radius FractureNCT05722808
What is the Rate of Surgical Treatment in Adult Patients With Displaced Distal Radius Fractures Managed According to the Danish National Clinical Practice Guidelines? - A Single Center Retrospective Cohort Study
An observational study of Distal Radius Fracture, run by Nordsjaellands Hospital at 1 site in Denmark.
Trial summary
Through this study we aim to investigate the rate of DRFs initially treated with successful closed reduction (to an acceptable position, then immobilized in a plaster cast), that re-displace and end up requiring surgery. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Distal Radius Fracture
- How many people
- 1,000 participants
- Where
- 1 siteDenmark
- Study dates
- 1 Jan 2018to 31 Dec 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Adult patients with displaced DRFs treated at North Zealand Hospital from 1.1.2018 to 31.12.2019.
Who may be able to join
None listed.
Who cannot join
- Concomitant fracture of the ulna (except ulnar styloid process' fractures)
- Non-displaced DRFs
- Multiple trauma patients
- Ipsilateral upper extremity fractures, interfering with the treatment of the DRF
Trial locations and contacts
1 site in 1 country.
About this study
Through this study we aim to investigate the rate of DRFs initially treated with successful closed reduction (to an acceptable position, then immobilized in a plaster cast), that re-displace and end up requiring surgery.
This study will clarify the incidence of DRFs where surgical intervention could potentially be avoided if the initial closed reduction lasted until sufficient bone healing was attained. As DRFs are the most common fracture of the adult population treated in the Danish emergency departments, the aim of this study is to examine the amount of people with DRFs that could potentially avoid surgery and thereby lowering the cost to the health care system, as well as save the patient invasive surgery. Furthermore, we expect to classify which specific types of fractures according to Arbeitsgemeinschaft für Osteosynthesefragen/ Orthopaedic Trauma Association (AO/OTA) classification system have a high or low incidence of secondary surgery after primary closed reduction.
Read the detailed description
Study rational Only a limited number of orthopedic national clinical practice guidelines (NCPG) exist in Denmark. In 2013 a NCPG regarding the treatment of distal radius fractures (DRFs) was introduced in Denmark [1]. Without any major changes, it was updated in 2017, which is the latest version. Displaced distal radius fractures are very frequent in the adult population, with about 20.000 fractures pr. year, and the incidence is still increasing as the population ages [1, 2]. Two-thirds of DRFs in adults are displaced and require closed reduction [5]. Unfortunately, a large number of the reduced DRFs (32-64%) re-displace during cast immobilization within the first weeks after reduction [1]. According to the NCPG, it is considered good clinical practice to offer surgical treatment to patients of any age if a conventional wrist X-ray examination, following reduction of the fracture, reveals one or more of the radiological parameters described in figure 1. Furthermore, it is described as good clinical practice to be cautious about offering surgery to any patient with a low functional level, regardless of their age [1].
Background Each year about 20.000 adult patients are treated for DRF in the Danish emergency departments across the country [1]. Therefore, the DRF is the most frequently treated fracture among adults in the Danish healthcare system. As the population ages the number of DRF increases. Furthermore, the rate of surgical treatment of DRF increases independently, probably due to an international change towards more interventional treatment, favoring surgery above conservative treatment.
The years up to 2013, a change was observed in the surgical method concerning treatment of DRF. Internal fixation with a volar plate and screws increased at the expense of K-wires or external fixation. This change is seen even based on sparse literature evidence [1].
In the general population, the distribution of DRFs is bimodal, with the incidence peaks in young men - due to high energy trauma - and in postmenopausal women [2]. The majority of DRFs in the second group are caused by a fall on an outstretched hand from one's upright position, thus it is considered low-energy fractures. There is a significant predominance of women to whom this type of fracture occurs, which is connected to the fact that osteoporosis is an underlying cause [1]. In a Swedish study, Rundgren et al. found that 78% of all DRFs occurred in women [2], while it was found in a British study that the rate of women to men was 68:38 [3].
What does this trial add to current knowledge? Through this study we aim to investigate the rate of DRFs initially treated with successful closed reduction (to an acceptable position, then immobilized in a plaster cast), that re-displace and end up requiring surgery.
This study will clarify the incidence of DRFs where surgical intervention could potentially be avoided if the initial closed reduction lasted until sufficient bone healing was attained. As DRFs are the most common fracture of the adult population treated in the Danish emergency departments, the aim of this study is to examine the amount of people with DRFs that could potentially avoid surgery and thereby lowering the cost to the health care system, as well as save the patient invasive surgery. Furthermore, we expect to classify which specific types of fractures according to Arbeitsgemeinschaft für Osteosynthesefragen/ Orthopaedic Trauma Association (AO/OTA) classification system have a high or low incidence of secondary surgery after primary closed reduction.
Hypothesis We estimate the rate of surgical intervention of DRFs initially reduced to an acceptable position to be above 40%.
Aim The primary objective is to assess the rate of surgical treatment in adult patients with distal radial fractures, initially reduced successfully, managed in a single center according to the danish national clinical practice guidelines (NCPG).
Primary endpoint The purpose of this study, is to determine the frequency of secondary displacement of DRFs, initially treated with closed reduction and casting, but subsequently resulting in secondary surgery.
Secondary endpoints
- We aim to compare the rate of DRF displacement following primary closed reduction found in this study with a similar cohort treated in the Netherlands [4].
- We will perform a sub analysis of risk of secondary displacement according to the "Arbeitsgemeinschaft für Osteosynthesefragen" (AO) classification system for DRFs.
- We will determine the frequency of DRFs with unacceptable position, according to NCPG, following initial reduction that are treated non-surgical.
- We will determine the number of reductions performed at the initial visit in the emergency department following a distal radius fracture per patient.
Study Design This study will be conducted as a retrospective cohort study. In addition, outcomes from this study will be compared to outcomes from a comparable cohort from a previous retrospective study conducted in the Netherlands.
Population Adult patients with displaced DRFs treated at North Zealand Hospital (Nordsjællands Hospital, NOH) from 1.1.2018 to 31.12.2019.
Inclusion criteria Adult patients (≥18 years) with a DRF (DS252, DS252A, DS252B, DS252C and DS526), treated in the emergency department at NOH.
Exclusion criteria
- Concomitant fracture of the ulna (except ulnar styloid process' fractures)
- Non-displaced DRFs
- Multiple trauma patients
- Ipsilateral upper extremity fractures, interfering with the treatment of the DRF Method Data will be retrieved from the electronic patient records (Sundhedsplatformen (SP)). Potential participants will be identified by relevant diagnosis codes (DS252, DS252A, DS252B, DS252C and DS526), treated in the emergency department at NOH with closed reduction and an immobilizing cast from Jan 1st 2018 to Dec 31st 2019. We expect to include approximately 750 participants.
Data relevant to the above-described outcomes (i.e radiologic data, diagnosis/procedure codes and information from outpatient clinic visits) and data relevant for baseline characteristics will be extracted from patient electronic journals and transferred to investigators.
All extracted data will be transferred in pseudonymized form to an on-line data capturing system (REDCAP).
A team of orthopedic surgeons from the orthopedic department, NOH, will be asked to assess radiographic images from the initial visit to the emergency department to assess:
- Classification according to AO
- Non-displaced yes/no
- Radiographic measurements according to https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4641087/ (radial shortening, ulnar variance and volar/dorsal angulation)
A comparable cohort from an ongoing prospective study of DRFs, performed in the Netherlands, has been identified and the responsible researcher has been contacted and agreed to provide data for a comparison of data between the two groups. Data will be transferred in anonymized form to the primary investigator of this study and stored at a secure drive. The primary and secondary outcomes outlined above will be compared across the two cohorts.
Due to the study design, it will be possible to repeat the study in other hospitals and compare the results across the Danish emergency departments as well as international.
Statistical analysis Rate of DRF displacement, following initial reduction and cast treatment, is described with summary statistics.
Categorical and ordinal variables will be presented in percentages of the analyzed group. Continuous variables will be presented as mean followed by standard deviation. If continuous variables were not normally distributed, they will be presented as median with (25% and 75% quartiles) and log transformed before further analysis.
Categorical and ordinal variables are compared across groups using χ2 test (Pearson test). If a low number of expected frequencies is encountered, Fisher's exact test is used. For analysis of differences in continuous variables between groups, t-test will be carried out.
Multiple regression will be performed to identify possible associations between relevant clinical variants and risk of DRF displacement following initial reduction and cast treatment.
All statistical analyses will be performed in the SAS ® Studio 3.7 (SAS Institute Inc., Cary, NC, USA).
Statistical significance is defined as a probability (p-value) lower than 5%. Perspective The results of this study will allow us to clarify the number of patients with DRF where surgery could potentially be avoided. If a specific group of patients (determined radiologically due to AO-classifications) with larger risk of DRF displacement following initial reduction and cast treatment is identified, there would be a great incentive to improve the treatment of this group. In addition, the comparison with a cohorte from the Netherlands will allow us to identify international differences in treatment and diagnosis of DRFs. The results of this study may eventually lead to a reduction in surgical treatment of DRFs and thereby a possible reduction in cost in relation to DRF treatment to the society.
Quality control and monitoring The study will be conducted in accordance with the Helsinki declaration on "Ethical Principles for Medical Research Involving Human Subjects". The principles of Good Clinical Practice were followed throughout the study.
The STROBE guidelines will be followed in the initiation, data handling and presentation of the study.
The study protocol will be registered in the "The ISRCTN registry" before initiation.
No monitoring of the study is needed or planned of this retrospective cohort study. As the radiographic data for each patient has been evaluated by orthopedic consultant or senior registrar at least three times (initially in emergency department, day after at conference, in out-patient clinic and/or in the operating theater), we deem it highly unlikely that any new findings of clinical relevance should happen. In the unlikely event that a new clinical finding should be done we will consult the local radiograph responsible for orthopedic radiology at NOH.
Ethical considerations and data safety To protect the patient's privacy and integrity, data will be extrapolated from SP and pseudonymized, and it will not be possible to identify the individuals. This study will not have any effect on the treatment or outcome for the patient cohort, but will solely help to identify improvements of future treatments. This study will investigate potential areas of DRF treatment where improvement can be made to potentially avoid surgery in this large fragile population.
Ethical committee approval Before the study is initiated, approval from relevant ethical and data security agencies will be attained; "National Videnskabsetisk Komite, "Sundhedsdatastyrelsen, Forskerservice" and the Danish Data Protection Agency https://sundhedsdatastyrelsen.dk/da/forskerservice/ansog-om-data.
Recruitment As this is a retrospective cohort study there is no need to recruit patients, as the data needed can be found in the electronic patient records.
Economy There is no funding for this project, as well as no sponsors or donors. The primary investigator and all secondary investigators are unpaid and perform the investigation in their spare-time. Except the clinically responsible investigator, Jonas Askø Andersen, who is head of research in the Orthopedic department in North Zealand Hospital.
Dissemination of results We expect to complete the data- and statistical analysis in September 2022. At this point the data and conclusion will be published in an international or national peer-reviewed medical journal. Both positive, negative and inconclusive data will be published. In addition, data from the study will be presented at national and international conferences if possible. Should publication in a peer-reviewed journal not be possible, data will be published in an open access database.
Patient information As this study does not add new treatments or diagnostic methods to the patients involved and does not use individual or patient identifiable data, we have applied for data access without written consent from included individuals and therefore patient information has been deemed unnecessary.
References
- https://www.sst.dk/-/media/Udgivelser/2014/NKR-H%C3%A5ndledsn%C3%A6re-underarmsbrud/National-clinical-guideline-on-the-treatment-of-distal-radial-fractures.ashx?sc_lang=da\&hash=A867AD76B6ECFF5A7307A0C006E0938A
- Rundgren J, Bojan A, Navarro CM et. al., "Epidemiology, classification, treatment and mortality of distal radius fractures in adults: an observational study of 23,394 fractures from the national Swedish fracture register", BMC Musculoskeletal Disorders (2020) 21:88,
- Stirling ERB, Johnson NA, Dias JJ. Epidemiology of distal radius fractures in a geographically defined adult population. J Hand Surg Eur Vol. 2018;43(9):974-82.
- Berger AC , Barvelink B, Reijman M et. al., "Does circumferential casting prevent fracture redisplacement in reduced distal radius fractures? A retrospective multicentre study", Journal of Orthopaedic Surgery and Research (2021) 16:722
- Brogren E, Petanek M and Atroshi I, "Incidence and characteristics of distal radius fractures in a southern Swedish region", BMC Musculoskeletal Disorders
- Conditions
- Distal Radius Fracture
- Keywords
- Distal radius fracture
- Medical subject headings
- Wrist Fractures
What is being measured
The primary outcome is the main question the study is designed to answer.
Rate of surgical treatment
Rate of surgical treatment of distal radial fractures treated at North Zealand Hospital
Measured: Anticipated to be completed by 31/05-2023
Secondary outcomes (4)
Rate of fracture displacement following primary conservative treatment compared with Dutch cohort
Comparison of the rate of DRF displacement following primary closed reduction found in this study with a similar cohort treated in the Netherlands
Measured: Anticipated to be completed by 31/05-2023
sub analysis of risk of secondary displacement according to the "Arbeitsgemeinschaft für Osteosynthesefragen" (AO) classification system for DRFs
Measured: Anticipated to be completed by 31/05-2023
Incidence of distal radial fractures with unaccetable displacement following following initial reduction
Analysis of the frequency of distal radial fractures with unacceptable position, according to danish national guidelines, following initial reduction that are treated non-surgical
Measured: Anticipated to be completed by 31/05-2023
Number of reductions performed per patient with distal radial fractures
Measured: Anticipated to be completed by 31/05-2023
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Feb 2023
- Study start1 Jan 2018
- Primary completion31 Dec 2023 (estimated)
- Study completion31 Dec 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Distal Radius FractureStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 1,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Nordsjaellands Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05722808
- Sponsor's protocol ID
- 2214020
- Status last verified
- Jan 2023
- First submitted
- 1 Feb 2023
- Last updated
- 10 Feb 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Feb 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- What is the Rate of Surgical Treatment in Adult Patients With Displaced Distal Radius Fractures Managed According to the Danish National Clinical Practice Guidelines? - A Single Center Retrospective Cohort Study
- ClinicalTrials.gov ID
- NCT05722808
- Acronym / sponsor ID
- 2214020
- Conditions
- Distal Radius Fracture
- Keywords
- Distal radius fracture
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 1,000 participants (estimated)
- Lead sponsor
- Nordsjaellands HospitalUniversity, hospital or other
- Study start
- 1 Jan 2018 (actual)
- Primary completion
- 31 Dec 2023 (estimated)
- Study completion
- 31 Dec 2023 (estimated)
- First posted
- 10 Feb 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Through this study we aim to investigate the rate of DRFs initially treated with successful closed reduction (to an acceptable position, then immobilized in a plaster cast), that re-displace and end up requiring surgery.
This study will clarify the incidence of DRFs where surgical intervention could potentially be avoided if the initial closed reduction lasted until sufficient bone healing was attained. As DRFs are the most common fracture of the adult population treated in the Danish emergency departments, the aim of this study is to examine the amount of people with DRFs that could potentially avoid surgery and thereby lowering the cost to the health care system, as well as save the patient invasive surgery. Furthermore, we expect to classify which specific types of fractures according to Arbeitsgemeinschaft für Osteosynthesefragen/ Orthopaedic Trauma Association (AO/OTA) classification system have a high or low incidence of secondary surgery after primary closed reduction.
Detailed description
Study rational Only a limited number of orthopedic national clinical practice guidelines (NCPG) exist in Denmark. In 2013 a NCPG regarding the treatment of distal radius fractures (DRFs) was introduced in Denmark [1]. Without any major changes, it was updated in 2017, which is the latest version. Displaced distal radius fractures are very frequent in the adult population, with about 20.000 fractures pr. year, and the incidence is still increasing as the population ages [1, 2]. Two-thirds of DRFs in adults are displaced and require closed reduction [5]. Unfortunately, a large number of the reduced DRFs (32-64%) re-displace during cast immobilization within the first weeks after reduction [1]. According to the NCPG, it is considered good clinical practice to offer surgical treatment to patients of any age if a conventional wrist X-ray examination, following reduction of the fracture, reveals one or more of the radiological parameters described in figure 1. Furthermore, it is described as good clinical practice to be cautious about offering surgery to any patient with a low functional level, regardless of their age [1].
Background Each year about 20.000 adult patients are treated for DRF in the Danish emergency departments across the country [1]. Therefore, the DRF is the most frequently treated fracture among adults in the Danish healthcare system. As the population ages the number of DRF increases. Furthermore, the rate of surgical treatment of DRF increases independently, probably due to an international change towards more interventional treatment, favoring surgery above conservative treatment.
The years up to 2013, a change was observed in the surgical method concerning treatment of DRF. Internal fixation with a volar plate and screws increased at the expense of K-wires or external fixation. This change is seen even based on sparse literature evidence [1].
In the general population, the distribution of DRFs is bimodal, with the incidence peaks in young men - due to high energy trauma - and in postmenopausal women [2]. The majority of DRFs in the second group are caused by a fall on an outstretched hand from one's upright position, thus it is considered low-energy fractures. There is a significant predominance of women to whom this type of fracture occurs, which is connected to the fact that osteoporosis is an underlying cause [1]. In a Swedish study, Rundgren et al. found that 78% of all DRFs occurred in women [2], while it was found in a British study that the rate of women to men was 68:38 [3].
What does this trial add to current knowledge? Through this study we aim to investigate the rate of DRFs initially treated with successful closed reduction (to an acceptable position, then immobilized in a plaster cast), that re-displace and end up requiring surgery.
This study will clarify the incidence of DRFs where surgical intervention could potentially be avoided if the initial closed reduction lasted until sufficient bone healing was attained. As DRFs are the most common fracture of the adult population treated in the Danish emergency departments, the aim of this study is to examine the amount of people with DRFs that could potentially avoid surgery and thereby lowering the cost to the health care system, as well as save the patient invasive surgery. Furthermore, we expect to classify which specific types of fractures according to Arbeitsgemeinschaft für Osteosynthesefragen/ Orthopaedic Trauma Association (AO/OTA) classification system have a high or low incidence of secondary surgery after primary closed reduction.
Hypothesis We estimate the rate of surgical intervention of DRFs initially reduced to an acceptable position to be above 40%.
Aim The primary objective is to assess the rate of surgical treatment in adult patients with distal radial fractures, initially reduced successfully, managed in a single center according to the danish national clinical practice guidelines (NCPG).
Primary endpoint The purpose of this study, is to determine the frequency of secondary displacement of DRFs, initially treated with closed reduction and casting, but subsequently resulting in secondary surgery.
Secondary endpoints
- We aim to compare the rate of DRF displacement following primary closed reduction found in this study with a similar cohort treated in the Netherlands [4].
- We will perform a sub analysis of risk of secondary displacement according to the "Arbeitsgemeinschaft für Osteosynthesefragen" (AO) classification system for DRFs.
- We will determine the frequency of DRFs with unacceptable position, according to NCPG, following initial reduction that are treated non-surgical.
- We will determine the number of reductions performed at the initial visit in the emergency department following a distal radius fracture per patient.
Study Design This study will be conducted as a retrospective cohort study. In addition, outcomes from this study will be compared to outcomes from a comparable cohort from a previous retrospective study conducted in the Netherlands.
Population Adult patients with displaced DRFs treated at North Zealand Hospital (Nordsjællands Hospital, NOH) from 1.1.2018 to 31.12.2019.
Inclusion criteria Adult patients (≥18 years) with a DRF (DS252, DS252A, DS252B, DS252C and DS526), treated in the emergency department at NOH.
Exclusion criteria
- Concomitant fracture of the ulna (except ulnar styloid process' fractures)
- Non-displaced DRFs
- Multiple trauma patients
- Ipsilateral upper extremity fractures, interfering with the treatment of the DRF Method Data will be retrieved from the electronic patient records (Sundhedsplatformen (SP)). Potential participants will be identified by relevant diagnosis codes (DS252, DS252A, DS252B, DS252C and DS526), treated in the emergency department at NOH with closed reduction and an immobilizing cast from Jan 1st 2018 to Dec 31st 2019. We expect to include approximately 750 participants.
Data relevant to the above-described outcomes (i.e radiologic data, diagnosis/procedure codes and information from outpatient clinic visits) and data relevant for baseline characteristics will be extracted from patient electronic journals and transferred to investigators.
All extracted data will be transferred in pseudonymized form to an on-line data capturing system (REDCAP).
A team of orthopedic surgeons from the orthopedic department, NOH, will be asked to assess radiographic images from the initial visit to the emergency department to assess:
- Classification according to AO
- Non-displaced yes/no
- Radiographic measurements according to https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4641087/ (radial shortening, ulnar variance and volar/dorsal angulation)
A comparable cohort from an ongoing prospective study of DRFs, performed in the Netherlands, has been identified and the responsible researcher has been contacted and agreed to provide data for a comparison of data between the two groups. Data will be transferred in anonymized form to the primary investigator of this study and stored at a secure drive. The primary and secondary outcomes outlined above will be compared across the two cohorts.
Due to the study design, it will be possible to repeat the study in other hospitals and compare the results across the Danish emergency departments as well as international.
Statistical analysis Rate of DRF displacement, following initial reduction and cast treatment, is described with summary statistics.
Categorical and ordinal variables will be presented in percentages of the analyzed group. Continuous variables will be presented as mean followed by standard deviation. If continuous variables were not normally distributed, they will be presented as median with (25% and 75% quartiles) and log transformed before further analysis.
Categorical and ordinal variables are compared across groups using χ2 test (Pearson test). If a low number of expected frequencies is encountered, Fisher's exact test is used. For analysis of differences in continuous variables between groups, t-test will be carried out.
Multiple regression will be performed to identify possible associations between relevant clinical variants and risk of DRF displacement following initial reduction and cast treatment.
All statistical analyses will be performed in the SAS ® Studio 3.7 (SAS Institute Inc., Cary, NC, USA).
Statistical significance is defined as a probability (p-value) lower than 5%. Perspective The results of this study will allow us to clarify the number of patients with DRF where surgery could potentially be avoided. If a specific group of patients (determined radiologically due to AO-classifications) with larger risk of DRF displacement following initial reduction and cast treatment is identified, there would be a great incentive to improve the treatment of this group. In addition, the comparison with a cohorte from the Netherlands will allow us to identify international differences in treatment and diagnosis of DRFs. The results of this study may eventually lead to a reduction in surgical treatment of DRFs and thereby a possible reduction in cost in relation to DRF treatment to the society.
Quality control and monitoring The study will be conducted in accordance with the Helsinki declaration on "Ethical Principles for Medical Research Involving Human Subjects". The principles of Good Clinical Practice were followed throughout the study.
The STROBE guidelines will be followed in the initiation, data handling and presentation of the study.
The study protocol will be registered in the "The ISRCTN registry" before initiation.
No monitoring of the study is needed or planned of this retrospective cohort study. As the radiographic data for each patient has been evaluated by orthopedic consultant or senior registrar at least three times (initially in emergency department, day after at conference, in out-patient clinic and/or in the operating theater), we deem it highly unlikely that any new findings of clinical relevance should happen. In the unlikely event that a new clinical finding should be done we will consult the local radiograph responsible for orthopedic radiology at NOH.
Ethical considerations and data safety To protect the patient's privacy and integrity, data will be extrapolated from SP and pseudonymized, and it will not be possible to identify the individuals. This study will not have any effect on the treatment or outcome for the patient cohort, but will solely help to identify improvements of future treatments. This study will investigate potential areas of DRF treatment where improvement can be made to potentially avoid surgery in this large fragile population.
Ethical committee approval Before the study is initiated, approval from relevant ethical and data security agencies will be attained; "National Videnskabsetisk Komite, "Sundhedsdatastyrelsen, Forskerservice" and the Danish Data Protection Agency https://sundhedsdatastyrelsen.dk/da/forskerservice/ansog-om-data.
Recruitment As this is a retrospective cohort study there is no need to recruit patients, as the data needed can be found in the electronic patient records.
Economy There is no funding for this project, as well as no sponsors or donors. The primary investigator and all secondary investigators are unpaid and perform the investigation in their spare-time. Except the clinically responsible investigator, Jonas Askø Andersen, who is head of research in the Orthopedic department in North Zealand Hospital.
Dissemination of results We expect to complete the data- and statistical analysis in September 2022. At this point the data and conclusion will be published in an international or national peer-reviewed medical journal. Both positive, negative and inconclusive data will be published. In addition, data from the study will be presented at national and international conferences if possible. Should publication in a peer-reviewed journal not be possible, data will be published in an open access database.
Patient information As this study does not add new treatments or diagnostic methods to the patients involved and does not use individual or patient identifiable data, we have applied for data access without written consent from included individuals and therefore patient information has been deemed unnecessary.
References
- https://www.sst.dk/-/media/Udgivelser/2014/NKR-H%C3%A5ndledsn%C3%A6re-underarmsbrud/National-clinical-guideline-on-the-treatment-of-distal-radial-fractures.ashx?sc_lang=da\&hash=A867AD76B6ECFF5A7307A0C006E0938A
- Rundgren J, Bojan A, Navarro CM et. al., "Epidemiology, classification, treatment and mortality of distal radius fractures in adults: an observational study of 23,394 fractures from the national Swedish fracture register", BMC Musculoskeletal Disorders (2020) 21:88,
- Stirling ERB, Johnson NA, Dias JJ. Epidemiology of distal radius fractures in a geographically defined adult population. J Hand Surg Eur Vol. 2018;43(9):974-82.
- Berger AC , Barvelink B, Reijman M et. al., "Does circumferential casting prevent fracture redisplacement in reduced distal radius fractures? A retrospective multicentre study", Journal of Orthopaedic Surgery and Research (2021) 16:722
- Brogren E, Petanek M and Atroshi I, "Incidence and characteristics of distal radius fractures in a southern Swedish region", BMC Musculoskeletal Disorders
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Adult patients with displaced DRFs treated at North Zealand Hospital from 1.1.2018 to 31.12.2019.
Key inclusion criteria (0 listed)
Key exclusion criteria (4 listed)
- Concomitant fracture of the ulna (except ulnar styloid process' fractures)
- Non-displaced DRFs
- Multiple trauma patients
- Ipsilateral upper extremity fractures, interfering with the treatment of the DRF
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Rate of surgical treatment
Time frame: Anticipated to be completed by 31/05-2023
Rate of surgical treatment of distal radial fractures treated at North Zealand Hospital
4 secondary outcomes
Rate of fracture displacement following primary conservative treatment compared with Dutch cohort
Time frame: Anticipated to be completed by 31/05-2023
sub analysis of risk of secondary displacement according to the "Arbeitsgemeinschaft für Osteosynthesefragen" (AO) classification system for DRFs
Time frame: Anticipated to be completed by 31/05-2023
Incidence of distal radial fractures with unaccetable displacement following following initial reduction
Time frame: Anticipated to be completed by 31/05-2023
Number of reductions performed per patient with distal radial fractures
Time frame: Anticipated to be completed by 31/05-2023
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Feb 2023.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Distal Radius Fracture, run by Nordsjaellands Hospital at 1 site in Denmark.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 0 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 10 Feb 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Rate of surgical treatment (time frame: Anticipated to be completed by 31/05-2023). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Feb 2023.