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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).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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
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

Other trials in Turkey (Türkiye)

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
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 groups in NCT06753656
Study groupRoleWhat they receive
Minimally Invasive SurgeryExperimentalClosed reduction of the fracture without opening the fracture site
Receives: Procedure: Minimally Invasive Surgery
Open SurgeryActive comparatoropen 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.

  1. 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

  2. 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)
  1. 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

  2. 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.

  1. First posted31 Dec 2024
  2. Study start1 Oct 2022
  3. Primary completion1 Dec 2023
  4. Study completion1 Dec 2024

Resources

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)
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

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.

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