Comparison of Patients Who Underwent Open and Minimally Invasive Fixation in Lateral Malleolar Fractures

NCT ID: NCT06753656

Last Updated: 2025-01-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-10-01

Study Completion Date

2024-12-01

Brief Summary

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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

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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

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Lateral Malleolus Fracture Minimally Invasive Surgical Procedure Postoperative Pain Patient Discharge

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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.
Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors
Patients will be informed about both surgical techniques. Informed consent will be obtained. Accepting patients will be included in the study. Which group the patients are in will be masked. The surgical group in the follow-up will be explained.

Outcome assessors were masked. Outcome assessors are senior surgeon and radiology doctor. Scoring will be taken by the senior surgeon. Radiological measurements will be performed at different times by the radiology doctor and the senior surgeon.

Study Groups

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Minimally Invasive Surgery

Closed reduction of the fracture without opening the fracture site

Group Type EXPERIMENTAL

Minimally Invasive Surgery

Intervention Type PROCEDURE

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.

Open Surgery

open reduction of the fracture by opening the fracture site

Group Type ACTIVE_COMPARATOR

Open Surgery

Intervention Type PROCEDURE

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.

Interventions

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Open 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.

Intervention Type PROCEDURE

Minimally Invasive 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.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* 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

Exclusion Criteria

* 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
* 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
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Giresun University

OTHER

Sponsor Role lead

Responsible Party

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Emre Kurt

Principal Investigator, Medical Doctor, Orthopaedics and Traumatology,

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kürşad Aytekin, M.D.

Role: STUDY_DIRECTOR

Giresun University

Locations

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Giresun University Faculty of Medicine-Giresun Training and Research Hospital

Giresun, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Ordu University CREC 2022/229

Identifier Type: -

Identifier Source: org_study_id

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