Lateral Malleolus FractureNCT06753656
Comparison of Patients Who Underwent Open and Minimally Invasive Fixation in Lateral Malleolar Fractures
A study testing Open Surgery and Minimally Invasive Surgery in people with Lateral Malleolus Fracture and Minimally Invasive Surgical Procedure, run by Giresun University at 1 site in Turkey (Türkiye).
Trial summary
The aim of this study was to compare the postoperative clinical, functional and radiological results of two different surgical methods, minimally invasive percutaneous plate osteosynthesis method and open reduction-internal fixation method, for lateral malleolus fractures in patients presenting with ankle fractures. Read more about this study
- Who is it for?
- Ages 18 to 90 yearsHealthy volunteers can take part
- Conditions the study is for
- Lateral Malleolus Fracture, Minimally Invasive Surgical Procedure, Postoperative Pain
- What is being tested?
- Open Surgery and Minimally Invasive Surgery
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 68 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Oct 2022to 1 Dec 2024
- Phase
- Interventional
- 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 to 90 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- being a volunteer,
- closed distal fibular epiphysis,
- Lateral malleolus fractures operated for Weber type B or C fractures,
- patients with regular follow-up in outpatient clinic
Who cannot join
- open fractures
- fractures accompanied by pylon fractures,
- fractures accompanied by talus fractures,
- patients with a previous fracture/surgery of the same or another ankle,
- ankles accompanied by arthrosis,
- pathological fractures
Show all 11Show fewer
- multitrauma or polytrauma patients,
- those with psychiatric or neurological diseases,
- illiterate patients,
- congenital or acquired deformity of the lower extremities
- Patients who could not be reduced intraoperatively closed and who underwent open surgery
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Giresun University Faculty of Medicine-Giresun Training and Research Hospital
Giresun, 28200
About this study
Official title: Prospective Randomised Controlled Trial Evaluating the Outcomes of Open Reduction-Internal Fixation With Minimally Invasive Percutaneous Plate Osteosynthesis in Lateral Malleolus Fractures
The aim of this study was to compare the postoperative clinical, functional and radiological results of two different surgical methods, minimally invasive percutaneous plate osteosynthesis method and open reduction-internal fixation method, for lateral malleolus fractures in patients presenting with ankle fractures.
Read the detailed description
The study is a prospective randomized controlled clinical trial planned to be conducted at the Republic of Turkey Ministry of Health, Giresun University Faculty of Medicine, Giresun Training and Research Hospital, Department of Orthopedics and Traumatology.
The study includes patients who will undergo surgery for lateral malleolus fractures. No additional tests will be requested outside of routine clinical, radiological, and laboratory evaluations required during surgery, hospitalization, and outpatient follow-ups.
The routine treatment protocol for patients undergoing surgery for lateral malleolus fractures in clinic is as follows:
- A detailed medical history is obtained, followed by systemic and local examinations.
- Radiological evaluations, including comparative ankle radiographs (Anterior-Posterior, Lateral, and Mortise views) and computed tomography (CT) scans, are performed.
- The affected ankle is placed in a splint. Elevation and cold application are performed. Embolism prophylaxis is administered with enoxaparin.
- Anesthesia preparation is performed. The splint is removed daily for examination, and surgery is performed once skin folds are appropriate.
- Post-surgical and outpatient follow-ups include routine ankle radiographs.
- Prophylactic antibiotics are administered preoperatively.
- Analgesics, including paracetamol, non-steroidal anti-inflammatory drugs (NSAIDs), and opioids, are administered based on the patient's pain level, provided there are no contraindications.
- After surgical site monitoring, antibiotic prophylaxis, and analgesia control, the patient is discharged.
- Postoperative follow-ups are scheduled for the 2nd week, 4th week, 6th week, 3rd month, 6th month, and 1st year.
- For the first two weeks postoperatively, dressings are performed every other day, and sutures are removed during outpatient control.
- Patients walk with bilateral crutches non-weight bearing for the first 6 weeks. If syndesmosis screws are used, they are removed with a day-case hospitalization under local anesthesia at the end of the 6th week.
- Partial weight-bearing begins after the 6th week, and the load is progressively increased weekly. Crutches are discontinued 3 months postoperatively.
- Ankle range-of-motion exercises are planned and initiated by the attending surgeon before discharge.
- During outpatient follow-ups, the ankle is re-examined, and any patient complaints are evaluated and managed with appropriate investigations and treatments.
In patients who consent to participate in the study, the following data will be collected:
- Demographic data: Gender, age, education level, occupation, height, body weight, body mass index (BMI), affected side, lateralization, diagnosis, smoking status, alcohol use, comorbidities, and medications.
- Follow-up data: Fracture etiology, time of fracture occurrence, fracture mechanism, soft tissue classification (Ostern-Tscherne), fracture type based on Weber and Lauge-Hansen classifications, preoperative hospitalization duration, time of surgery, type and duration of anesthesia, surgical technique, surgical duration, syndesmosis fixation, tourniquet use (and duration), fluoroscopy frequency and duration, use of drains (and removal time), postoperative hospitalization duration, use of tranexamic acid for bleeding control, discharge date, medications used during hospitalization and post-discharge, postoperative splint use, and syndesmosis screw removal timing if applicable.
Surgical approach:
Patients undergoing lateral malleolus surgery are operated on in the supine position under anesthesia with the hip elevated. A tourniquet is applied. Following the preparation of the lower extremity with povidone-iodine, the surgical method-open or minimally invasive-is selected based on the surgeon's experience.
- In the open approach: A longitudinal incision is made over the lateral malleolus, followed by sharp dissection down to the bone. The fracture is reduced under direct visualization and fixed with a plate and screws.
- In the minimally invasive method: A 2-3 cm longitudinal incision is made distal to the lateral malleolus to allow for plate placement. A periosteal elevator is used to create a pathway for the plate. The fracture is reduced in a closed manner using reduction clamps, and the plate position is confirmed fluoroscopically. A second longitudinal incision is made proximal to the fracture, and the plate is temporarily fixed with Kirschner wires. The plate is then used as an external guide, with screws placed through mini-incisions. The fracture is fixed with the plate-screw system in a minimally invasive manner.
- Regardless of the fixation method, the surgical site is irrigated with saline, incisions are closed with sutures, dressings are applied, and a short-leg splint is used to facilitate soft tissue healing. The operation is then concluded.
Radiological assessment:
Fracture classification will be performed based on direct radiographs. Additionally, radiographic parameters, including medial clear space, tibiofibular overlapping, tibiofibular clear space, talar tilt, and talocrural angle, will be measured and compared with the unaffected ankle.
Planned clinical scoring scales and evaluation timelines:
- Numeric Pain Rating Scale (NPRS): Preoperatively, and postoperatively 8th hour, 24th hour, 2nd week, 4th week, 6th week, 3rd month, 6th month, and 1st year
- AOFAS (American Orthopaedic Foot and Ankle Society) Ankle Score: Postoperatively 3rd month, 6th month, and 1st year
- Conditions
- Lateral Malleolus Fracture, Minimally Invasive Surgical Procedure, Postoperative Pain, Patient Discharge
- Being tested
- Open Surgery, Minimally Invasive Surgery
- Keywords
- Lateral Malleolus Fractures, Minimally Invasive Surgery, Postoperative Pain
- Medical subject headings
- Ankle Fractures, Pain, Postoperative
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Open SurgeryProcedure or surgery
Open surgery technique: A longitudinal incision is made over the lateral malleolus, followed by sharp dissection down to the bone. The fracture is reduced under direct visualization and fixed with a plate and screws.
Minimally Invasive SurgeryProcedure or surgery
Closed surgery technique: A 2-3 cm longitudinal incision is made distal to the lateral malleolus to allow for plate placement. A periosteal elevator is used to create a pathway for the plate. The fracture is reduced in a closed manner using reduction clamps, and the plate position is confirmed fluoroscopically. A second longitudinal incision is made proximal to the fracture, and the plate is temporarily fixed with Kirschner wires. The plate is then used as an external guide, with screws placed through mini-incisions. The fracture is fixed with the plate-screw system in a minimally invasive manner.
| Study group | Role | What they receive |
|---|---|---|
| Minimally Invasive Surgery | Experimental | Closed reduction of the fracture without opening the fracture site Receives: Procedure: Minimally Invasive Surgery |
| Open Surgery | Active comparator | open reduction of the fracture by opening the fracture site Receives: Procedure: Open Surgery |
What is being measured
The primary outcome is the main question the study is designed to answer.
Post operative Pain
Patients were analysed for pain scores according to the numeric pain rating scale(NPRS) for the following periods
Measured: Preoperatively and postoperatively 8th hour, 24th hour, 2nd week, 4th week, 3rd month, 6th month and 1st year
Patient discharge time
Preoperative, postoperative and total hospital stay and discharge times of the patients were recorded.
Measured: Up to 12 months
Secondary outcomes (2)
The number and duration of fluoroscopy
The number and duration of fluoroscopies used during the entire surgery for each patient is recorded.
Measured: Postoperative 1st day
Functional score
AOFAS scores were obtained at the follow-up visits of the patients at the following times
Measured: Postoperatively 3rd month, 6th month and 1st year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 Dec 2024
- Study start1 Oct 2022
- Primary completion1 Dec 2023
- Study completion1 Dec 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Lateral Malleolus 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Randomisation was performed before the first patient was included in the study. Patients were numbered according to the order of hospitalisation. According to these numbers, the surgical technique was applied to the patients according to the surgical technique group.
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 68 participants (actual)
Sponsor and investigators
- Lead sponsor
- Giresun University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Emre Kurt, Giresun University
- Investigators
- Kürşad Aytekin, M.D., Study director, Giresun University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06753656
- Sponsor's protocol ID
- Ordu University CREC 2022/229
- Status last verified
- Jan 2025
- First submitted
- 18 Dec 2024
- Last updated
- 6 Jan 2025
- 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 6 Jan 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Prospective Randomised Controlled Trial Evaluating the Outcomes of Open Reduction-Internal Fixation With Minimally Invasive Percutaneous Plate Osteosynthesis in Lateral Malleolus Fractures
- ClinicalTrials.gov ID
- NCT06753656
- Acronym / sponsor ID
- Ordu University CREC 2022/229
- Conditions
- Lateral Malleolus Fracture, Minimally Invasive Surgical Procedure, Postoperative Pain, Patient Discharge
- Keywords
- Lateral Malleolus Fractures, Minimally Invasive Surgery, Postoperative Pain
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 68 participants (actual)
- Lead sponsor
- Giresun UniversityUniversity, hospital or other
- Study start
- 1 Oct 2022 (actual)
- Primary completion
- 1 Dec 2023 (actual)
- Study completion
- 1 Dec 2024 (actual)
- First posted
- 31 Dec 2024 (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.
The aim of this study was to compare the postoperative clinical, functional and radiological results of two different surgical methods, minimally invasive percutaneous plate osteosynthesis method and open reduction-internal fixation method, for lateral malleolus fractures in patients presenting with ankle fractures.
Detailed description
The study is a prospective randomized controlled clinical trial planned to be conducted at the Republic of Turkey Ministry of Health, Giresun University Faculty of Medicine, Giresun Training and Research Hospital, Department of Orthopedics and Traumatology.
The study includes patients who will undergo surgery for lateral malleolus fractures. No additional tests will be requested outside of routine clinical, radiological, and laboratory evaluations required during surgery, hospitalization, and outpatient follow-ups.
The routine treatment protocol for patients undergoing surgery for lateral malleolus fractures in clinic is as follows:
- A detailed medical history is obtained, followed by systemic and local examinations.
- Radiological evaluations, including comparative ankle radiographs (Anterior-Posterior, Lateral, and Mortise views) and computed tomography (CT) scans, are performed.
- The affected ankle is placed in a splint. Elevation and cold application are performed. Embolism prophylaxis is administered with enoxaparin.
- Anesthesia preparation is performed. The splint is removed daily for examination, and surgery is performed once skin folds are appropriate.
- Post-surgical and outpatient follow-ups include routine ankle radiographs.
- Prophylactic antibiotics are administered preoperatively.
- Analgesics, including paracetamol, non-steroidal anti-inflammatory drugs (NSAIDs), and opioids, are administered based on the patient's pain level, provided there are no contraindications.
- After surgical site monitoring, antibiotic prophylaxis, and analgesia control, the patient is discharged.
- Postoperative follow-ups are scheduled for the 2nd week, 4th week, 6th week, 3rd month, 6th month, and 1st year.
- For the first two weeks postoperatively, dressings are performed every other day, and sutures are removed during outpatient control.
- Patients walk with bilateral crutches non-weight bearing for the first 6 weeks. If syndesmosis screws are used, they are removed with a day-case hospitalization under local anesthesia at the end of the 6th week.
- Partial weight-bearing begins after the 6th week, and the load is progressively increased weekly. Crutches are discontinued 3 months postoperatively.
- Ankle range-of-motion exercises are planned and initiated by the attending surgeon before discharge.
- During outpatient follow-ups, the ankle is re-examined, and any patient complaints are evaluated and managed with appropriate investigations and treatments.
In patients who consent to participate in the study, the following data will be collected:
- Demographic data: Gender, age, education level, occupation, height, body weight, body mass index (BMI), affected side, lateralization, diagnosis, smoking status, alcohol use, comorbidities, and medications.
- Follow-up data: Fracture etiology, time of fracture occurrence, fracture mechanism, soft tissue classification (Ostern-Tscherne), fracture type based on Weber and Lauge-Hansen classifications, preoperative hospitalization duration, time of surgery, type and duration of anesthesia, surgical technique, surgical duration, syndesmosis fixation, tourniquet use (and duration), fluoroscopy frequency and duration, use of drains (and removal time), postoperative hospitalization duration, use of tranexamic acid for bleeding control, discharge date, medications used during hospitalization and post-discharge, postoperative splint use, and syndesmosis screw removal timing if applicable.
Surgical approach:
Patients undergoing lateral malleolus surgery are operated on in the supine position under anesthesia with the hip elevated. A tourniquet is applied. Following the preparation of the lower extremity with povidone-iodine, the surgical method-open or minimally invasive-is selected based on the surgeon's experience.
- In the open approach: A longitudinal incision is made over the lateral malleolus, followed by sharp dissection down to the bone. The fracture is reduced under direct visualization and fixed with a plate and screws.
- In the minimally invasive method: A 2-3 cm longitudinal incision is made distal to the lateral malleolus to allow for plate placement. A periosteal elevator is used to create a pathway for the plate. The fracture is reduced in a closed manner using reduction clamps, and the plate position is confirmed fluoroscopically. A second longitudinal incision is made proximal to the fracture, and the plate is temporarily fixed with Kirschner wires. The plate is then used as an external guide, with screws placed through mini-incisions. The fracture is fixed with the plate-screw system in a minimally invasive manner.
- Regardless of the fixation method, the surgical site is irrigated with saline, incisions are closed with sutures, dressings are applied, and a short-leg splint is used to facilitate soft tissue healing. The operation is then concluded.
Radiological assessment:
Fracture classification will be performed based on direct radiographs. Additionally, radiographic parameters, including medial clear space, tibiofibular overlapping, tibiofibular clear space, talar tilt, and talocrural angle, will be measured and compared with the unaffected ankle.
Planned clinical scoring scales and evaluation timelines:
- Numeric Pain Rating Scale (NPRS): Preoperatively, and postoperatively 8th hour, 24th hour, 2nd week, 4th week, 6th week, 3rd month, 6th month, and 1st year
- AOFAS (American Orthopaedic Foot and Ankle Society) Ankle Score: Postoperatively 3rd month, 6th month, and 1st year
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
- Model description
- Randomisation was performed before the first patient was included in the study. Patients were numbered according to the order of hospitalisation. According to these numbers, the surgical technique was applied to the patients according to the surgical technique group.
| Arm | Type | Receives |
|---|---|---|
| Minimally Invasive Surgery | Experimental | Procedure: Minimally Invasive SurgeryClosed reduction of the fracture without opening the fracture site |
| Open Surgery | Active comparator | Procedure: Open Surgeryopen reduction of the fracture by opening the fracture site |
Who may qualify
- Ages
- 18 to 90 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- being a volunteer,
- closed distal fibular epiphysis,
- Lateral malleolus fractures operated for Weber type B or C fractures,
- patients with regular follow-up in outpatient clinic
Key exclusion criteria (11 listed)
- open fractures
- fractures accompanied by pylon fractures,
- fractures accompanied by talus fractures,
- patients with a previous fracture/surgery of the same or another ankle,
- ankles accompanied by arthrosis,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Open SurgeryOpen surgery technique: A longitudinal incision is made over the lateral malleolus, followed by sharp dissection down to the bone. The fracture is reduced under direct visualization and fixed with a plate and screws. | Procedure or surgery | Open Surgery |
| Minimally Invasive SurgeryClosed surgery technique: A 2-3 cm longitudinal incision is made distal to the lateral malleolus to allow for plate placement. A periosteal elevator is used to create a pathway for the plate. The fracture is reduced in a closed manner using reduction clamps, and the plate position is confirmed fluoroscopically. A second longitudinal incision is made proximal to the fracture, and the plate is temporarily fixed with Kirschner wires. The plate is then used as an external guide, with screws placed through mini-incisions. The fracture is fixed with the plate-screw system in a minimally invasive manner. | Procedure or surgery | Minimally Invasive Surgery |
Primary outcome
Post operative Pain
Time frame: Preoperatively and postoperatively 8th hour, 24th hour, 2nd week, 4th week, 3rd month, 6th month and 1st year
Patients were analysed for pain scores according to the numeric pain rating scale(NPRS) for the following periods
Patient discharge time
Time frame: Up to 12 months
Preoperative, postoperative and total hospital stay and discharge times of the patients were recorded.
2 secondary outcomes
The number and duration of fluoroscopy
Time frame: Postoperative 1st day
Functional score
Time frame: Postoperatively 3rd month, 6th month and 1st year
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 6 Jan 2025.
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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.
Kürşad Aytekin, M.D. study director
Giresun University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Open Surgery and Minimally Invasive Surgery in people with Lateral Malleolus Fracture and Minimally Invasive Surgical Procedure, run by Giresun University at 1 site in Turkey (Türkiye).
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 4 inclusion and 11 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 6 Jan 2025. 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 Turkey (Türkiye). 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?
Post operative Pain (time frame: Preoperatively and postoperatively 8th hour, 24th hour, 2nd week, 4th week, 3rd month, 6th month and 1st year). The study lists 2 primary outcomes in all. 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 6 Jan 2025.