Clinical Decision MakingNCT05845437
On Adequacy of Referrals to Oral and Maxillofacial Surgery
An observational study of Clinical Decision Making and Tooth Extraction, run by Region Skane at 1 site in Sweden.
Trial summary
Currently, an ongoing generational shift of the dental community in Sweden originates from an increased number of retiring dentists. Meanwhile, a declining number of dental professionals puts a strain on the care system and reduces the availability of dental care to patients in need of treatment. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Clinical Decision Making, Tooth Extraction, Referral and Consultation
- How many people
- 624 participants
- Where
- 1 siteSweden
- Study dates
- 1 May 2023to 30 Sep 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 Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Total referred population
Who may be able to join
- Patients referred for dentoalveolar surgery during 2021.
Who cannot join
- Word of mouth refferals.
- Referrals send by patients.
- Referrals concerning lesions of the jaw and mucosa that are not of dental origin.
Trial locations and contacts
1 site in 1 country.
Sweden1 site
Department of oral and maxillofacial surgery
Lund, Skåne County, 22185
About this study
Official title: A Study on Adequacy of Referrals to Oral and Maxillofacial Surgery Departments in Southern Sweden - Are All Referrals Necessary
Currently, an ongoing generational shift of the dental community in Sweden originates from an increased number of retiring dentists. Meanwhile, a declining number of dental professionals puts a strain on the care system and reduces the availability of dental care to patients in need of treatment. With fewer experienced dentists, available to guide newly graduated dentists, an increased number of referrals to specialist care units might be a consequence. E.g. referrals to oral and maxillofacial departments originating from a need of assistance in more advanced cases of assessments, treatment planning and therapies. The decreasing number of dentists is also possible to negatively affect the recruitment to specialized dental units, which in turn further decreases treatment availability. When the need for dental care exceeds the capacity of the dental care providers, a possible solution might be to minimize the number of referrals possible to treat in general dentistry, thus prioritize patients truly in need of specialist care. Hence, a reduced waiting time and improved accessibility to an adequate treatment.
The aim of this study is to explore the suitability of referrals concerning exodontia to the departments of oral and maxillofacial surgery in southern Sweden. The primary objective is to assess the level of difficulty in referrals on dental extractions. Secondary objectives are assessments of outcome from treatment and comparison of the suggested treatment of the referral with the outcome. The hypothesis is that the level of difficulty of the required treatments in referrals to oral and maxillofacial departments in southern Sweden is low and constitutes a contributing factor to prolonged waiting queues in specialized dentistry.
Read the detailed description
The following study is a retrospective study wherein referral letters sent over the course of the months of January to December in 2021 to oral and maxillofacial surgery departments in Lund, Helsingborg and Kristianstad, Sweden will be consecutively collected and reviewed. After a a total screening of referrals concerning dentoalveolar surgery referrals that are related to or possibly related to exodontia will be included into the study. Each referral letter is going to be assessed by the following criteria:
- Patient chief complaint
- Patient's general health
- Tooth/teeth in question
- Clinical assessment
- Radiological assessment
- Diagnosis
- Reason for referral
- Requested treatment: extraction (open or closed), apical surgery, hemisection, consultation, unspecified
The data from referral letters will be compared with data in equivalent journal records of the treatment outcome in every referred case. Each journal record is going to be assessed by the following criteria:
- Patient chief complaint
- Patient's general health
- Tooth/teeth in question
- Clinical assessment
- Radiological assessment
- Diagnosis
- Treatment indication
- Outcome of referral;
- Treatment: extraction (open or closed), apical surgery, hemisection
- No treatment
The level of difficulty of each referred case is going to be measured by a comparison of the referral letters to equivalent patient journal and assessment of treatment outcome. The studied cases will be ranked into one of four categories, wherein categories 1-3 are considered as complicated.
- Patients whose general heath increases the risk of postoperative medical complications.
- Cases wherein exodontia cannot be carried out without elevating a surgical flap.
- Cases wherein exodontia can affect nearby anatomical structures (such as risk of sinus perforation and damage to the inferior alveolar nerve).
- Otherwise healthy patients where exodontia can be carried out by closed extraction without flap elevation.
Study rational
The recorded data will be analyzed for the level of difficulty, suitability to referral by a comparison with the judged level of difficulty and for the outcome from treatment. Comparisons will be made between the judged level of difficulty with the outcome and the suggested treatment of the referral with the outcome.
Statistical analysis
The sample constitutes of a total inclusion from a cohort limited in time, department and treatment method. The project is designed as an observational trial without control group. Thus, a power-analysis is not valued as necessary for this project.
Simple statistical analysis including mean, standard deviation and range will be used. The limit for statistical significance will be set to p<0.05. A two-sided p-value will be used. Statistical analysis of the data will be performed by use of SPSS - IBM Inc.
Ethical considerations
The study is to be performed in accordance with the 21 CFR, part 50 and the directives laid down in the declaration of Helsinki (Appendix 1 of the declaration, as adopted by the 18th World Medical Assembly, Tokyo, 1975, the 35th WMA, Venice 1983, and the 41st WM A, Hong, Kong 1989, the 48th WMA, Somerset West 1996, the 52nd WMA, Edinburgh 2000 and the clarifications 2002 and 2004).
The project has been submitted to a properly constituted independent Ethics Committee (EC), in agreement with national rules, for formal approval of the study conduct. The decision of the EC concerning the conduct of the study will be in writing to the Investigator and a copy of this decision is archived in the Investigator's Study File.
Patient data protection
The researcher will keep a patient identification list including sufficient information to link records, i.e. CRFs and hospital records. Swedish and local regulations for the handling of computerized data will be followed and described in the written patient information and identification of individual patient data will only be possible for the researcher. A list of the decoded social security numbers of the patients will be kept at the department of Oral and Maxillofacial Surgery, only accessible by the principal researcher.
Report and communication of results After completion of the study, the statistical analysis will be performed by the research group. These data will form the basis for a manuscript intended for publication in a medical journal within two years of the after the project is finished.
Significance and implementation
Adequate referrals are important to have the relatively more expensive specialist health-care units to work as effective as possible. Through a focus of having the best competence predesignated for the most advanced and difficult treatments, the availability and treatment cost will be kept at a desirable level. This is true from both a patient, a health-care provider and a society perspective.
The present study will evaluate the accuracy of the actual referrals in a 12-month time-span. The outcome will give guidance to decision makers in healthcare strategies. Hence, the outcome will, in the short coming future affect education of clinicians, specialist unit geographic establishment and governmental financial support to an improved suitability of health care resources.
The current project aims to clarify the benefits of directed adequate referrals to specialized units of Oral and Maxillofacial Surgery. By knowledge of how the level of existing referrals corresponds to the outcome and how they present, the health care optimization of specialized availability and referral directions will be supported. After publication of the results from the present study, the knowledge will be provided to key decision makers within health care systems.
- Conditions
- Clinical Decision Making, Tooth Extraction, Referral and Consultation, Surgery, Oral, Oral Surgical Procedures
- Keywords
- Surgery, Dental, Referrals, Relevance
What is being measured
The primary outcome is the main question the study is designed to answer.
Referral question
What is expected from the surgical unit?
Measured: 12 months
Secondary outcomes (3)
Performed treatment
What surgical treatment was given?
Measured: 12 months
Relevance
Was the treatment possible to perform at general dentistry?
Measured: 12 months
Relevance
Was there a discrepancy between expected treatment and performed treatment?
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 May 2023
- Study start1 May 2023
- Primary completion15 Sep 2023
- Study completion30 Sep 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Clinical Decision MakingStudies of the same condition, open and under way.
- More trials run by Region SkaneThe sponsor's other registered studies.
- 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
- 624 participants (actual)
Sponsor and investigators
- Lead sponsor
- Region Skane
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05845437
- Sponsor's protocol ID
- 2023-01379-01
- Other IDs
- 2023
- Status last verified
- Feb 2024
- First submitted
- 25 Apr 2023
- Last updated
- 29 Feb 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 Feb 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Study on Adequacy of Referrals to Oral and Maxillofacial Surgery Departments in Southern Sweden - Are All Referrals Necessary
- ClinicalTrials.gov ID
- NCT05845437
- Acronym / sponsor ID
- 2023-01379-01
- Conditions
- Clinical Decision Making, Tooth Extraction, Referral and Consultation, Surgery, Oral, Oral Surgical Procedures
- Keywords
- Surgery, Dental, Referrals, Relevance
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 624 participants (actual)
- Lead sponsor
- Region SkaneUniversity, hospital or other
- Study start
- 1 May 2023 (actual)
- Primary completion
- 15 Sep 2023 (actual)
- Study completion
- 30 Sep 2023 (actual)
- First posted
- 6 May 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.
Currently, an ongoing generational shift of the dental community in Sweden originates from an increased number of retiring dentists. Meanwhile, a declining number of dental professionals puts a strain on the care system and reduces the availability of dental care to patients in need of treatment. With fewer experienced dentists, available to guide newly graduated dentists, an increased number of referrals to specialist care units might be a consequence. E.g. referrals to oral and maxillofacial departments originating from a need of assistance in more advanced cases of assessments, treatment planning and therapies. The decreasing number of dentists is also possible to negatively affect the recruitment to specialized dental units, which in turn further decreases treatment availability. When the need for dental care exceeds the capacity of the dental care providers, a possible solution might be to minimize the number of referrals possible to treat in general dentistry, thus prioritize patients truly in need of specialist care. Hence, a reduced waiting time and improved accessibility to an adequate treatment.
The aim of this study is to explore the suitability of referrals concerning exodontia to the departments of oral and maxillofacial surgery in southern Sweden. The primary objective is to assess the level of difficulty in referrals on dental extractions. Secondary objectives are assessments of outcome from treatment and comparison of the suggested treatment of the referral with the outcome. The hypothesis is that the level of difficulty of the required treatments in referrals to oral and maxillofacial departments in southern Sweden is low and constitutes a contributing factor to prolonged waiting queues in specialized dentistry.
Detailed description
The following study is a retrospective study wherein referral letters sent over the course of the months of January to December in 2021 to oral and maxillofacial surgery departments in Lund, Helsingborg and Kristianstad, Sweden will be consecutively collected and reviewed. After a a total screening of referrals concerning dentoalveolar surgery referrals that are related to or possibly related to exodontia will be included into the study. Each referral letter is going to be assessed by the following criteria:
- Patient chief complaint
- Patient's general health
- Tooth/teeth in question
- Clinical assessment
- Radiological assessment
- Diagnosis
- Reason for referral
- Requested treatment: extraction (open or closed), apical surgery, hemisection, consultation, unspecified
The data from referral letters will be compared with data in equivalent journal records of the treatment outcome in every referred case. Each journal record is going to be assessed by the following criteria:
- Patient chief complaint
- Patient's general health
- Tooth/teeth in question
- Clinical assessment
- Radiological assessment
- Diagnosis
- Treatment indication
- Outcome of referral;
- Treatment: extraction (open or closed), apical surgery, hemisection
- No treatment
The level of difficulty of each referred case is going to be measured by a comparison of the referral letters to equivalent patient journal and assessment of treatment outcome. The studied cases will be ranked into one of four categories, wherein categories 1-3 are considered as complicated.
- Patients whose general heath increases the risk of postoperative medical complications.
- Cases wherein exodontia cannot be carried out without elevating a surgical flap.
- Cases wherein exodontia can affect nearby anatomical structures (such as risk of sinus perforation and damage to the inferior alveolar nerve).
- Otherwise healthy patients where exodontia can be carried out by closed extraction without flap elevation.
Study rational
The recorded data will be analyzed for the level of difficulty, suitability to referral by a comparison with the judged level of difficulty and for the outcome from treatment. Comparisons will be made between the judged level of difficulty with the outcome and the suggested treatment of the referral with the outcome.
Statistical analysis
The sample constitutes of a total inclusion from a cohort limited in time, department and treatment method. The project is designed as an observational trial without control group. Thus, a power-analysis is not valued as necessary for this project.
Simple statistical analysis including mean, standard deviation and range will be used. The limit for statistical significance will be set to p<0.05. A two-sided p-value will be used. Statistical analysis of the data will be performed by use of SPSS - IBM Inc.
Ethical considerations
The study is to be performed in accordance with the 21 CFR, part 50 and the directives laid down in the declaration of Helsinki (Appendix 1 of the declaration, as adopted by the 18th World Medical Assembly, Tokyo, 1975, the 35th WMA, Venice 1983, and the 41st WM A, Hong, Kong 1989, the 48th WMA, Somerset West 1996, the 52nd WMA, Edinburgh 2000 and the clarifications 2002 and 2004).
The project has been submitted to a properly constituted independent Ethics Committee (EC), in agreement with national rules, for formal approval of the study conduct. The decision of the EC concerning the conduct of the study will be in writing to the Investigator and a copy of this decision is archived in the Investigator's Study File.
Patient data protection
The researcher will keep a patient identification list including sufficient information to link records, i.e. CRFs and hospital records. Swedish and local regulations for the handling of computerized data will be followed and described in the written patient information and identification of individual patient data will only be possible for the researcher. A list of the decoded social security numbers of the patients will be kept at the department of Oral and Maxillofacial Surgery, only accessible by the principal researcher.
Report and communication of results After completion of the study, the statistical analysis will be performed by the research group. These data will form the basis for a manuscript intended for publication in a medical journal within two years of the after the project is finished.
Significance and implementation
Adequate referrals are important to have the relatively more expensive specialist health-care units to work as effective as possible. Through a focus of having the best competence predesignated for the most advanced and difficult treatments, the availability and treatment cost will be kept at a desirable level. This is true from both a patient, a health-care provider and a society perspective.
The present study will evaluate the accuracy of the actual referrals in a 12-month time-span. The outcome will give guidance to decision makers in healthcare strategies. Hence, the outcome will, in the short coming future affect education of clinicians, specialist unit geographic establishment and governmental financial support to an improved suitability of health care resources.
The current project aims to clarify the benefits of directed adequate referrals to specialized units of Oral and Maxillofacial Surgery. By knowledge of how the level of existing referrals corresponds to the outcome and how they present, the health care optimization of specialized availability and referral directions will be supported. After publication of the results from the present study, the knowledge will be provided to key decision makers within health care systems.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Total referred population
Key inclusion criteria (1 listed)
- Patients referred for dentoalveolar surgery during 2021.
Key exclusion criteria (3 listed)
- Word of mouth refferals.
- Referrals send by patients.
- Referrals concerning lesions of the jaw and mucosa that are not of dental origin.
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
Referral question
Time frame: 12 months
What is expected from the surgical unit?
3 secondary outcomes
Performed treatment
Time frame: 12 months
Relevance
Time frame: 12 months
Relevance
Time frame: 12 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Feb 2024.
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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 Clinical Decision Making and Tooth Extraction, run by Region Skane at 1 site in Sweden.
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 1 inclusion and 3 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: finished, as of the sponsor's last update on 29 Feb 2024. 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 Sweden. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Referral question (time frame: 12 months). 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 29 Feb 2024.