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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05991557
Other study ID # peroneus longus graft
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 1, 2023
Est. completion date December 2025

Study information

Verified date August 2023
Source Assiut University
Contact mahmoud sabra ahmed, resident doctor
Phone +0201006721501
Email ahmedsabra310@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to report the ankle and foot functions via American orthopedic foot and ankle society score (AOFAS), peronei muscle testing ,handheld dynamometer and radiological outcomes after harvesting autogenous peroneus longus tendons for ligaments reconstruction.


Description:

Using a Peroneus longus tendon (PLT) as an autograft is a common procedure and has been used previously for deltoid ligament reconstruction in flatfoot deformity correction . Recently, (PLT) is gaining popularity as a graft option in primary anterior cruciate ligament (ACL) reconstruction surgeries with biomechanical studies showing tensile strength and clinical outcomes comparable to quadrupled hamstring grafts. In addition to using PLT for isolated (ACL), it is also used in posterior cruciate ligament (PCL) reconstruction, medial collateral ligament reconstruction, posterolateral corner reconstruction of the knee, or knee multiple ligament injuries . The partial-thickness of the tendon has been used variably in knee ligament surgery.. Being a powerful muscle in plantar flexion and eversion of the foot, there might be associated ankle functional impairment. To the authors knowledge, there is a gap in science evaluating donor site morbidity. The aim of this study is to report the clinical and functional outcome of the donor site for better explanation of the cons and pros of using PLT as a graft in joint ligamentous injury .


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 54
Est. completion date December 2025
Est. primary completion date September 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: 1. clinical and radiological diaginsis of joint ligament injury and needs to ligament reconstruction . 2. people with asymptomatic ankle and foot pre and post injury Exclusion Criteria: 1. Associated ankle and/or foot fractures. 2. Associated hip or pelvic fractures 3. Abnormal ankle function pre-injury. 4. Contralateral limb fractures 5. Traumatic brain injury (TBI) that limits their ability to participate in their post-operative care; 6. Presence of neurological condition that result in spasticity or any abnormal lower limb muscles tone. 7. Any condition that would preclude the ability to comply with post-operative guidelines.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
peroneus longus autograft
Peroneus longus tendon graft will be harvested with a longitudinal skin incision at 2 to 3 cm (2 finger-breadths) above and 1 cm (1 finger-breadth) behind the lateral malleolus, followed by superficial fascia incision in line with skin incision followed by incision of the tendon sheath proximal to the retinaculum. The peroneus longus and peroneus brevis tendons will be then identified. The tendon division location marked at 2 to 3 cm above the level of the lateral malleolus.The peroneus longus tendon will be exposed on its posterolateral surface through the incision after carefully incising the fascia

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary peronei muscle strength testing using handheld dynamometer power of plantar flexion and eversion of foot and ankle preoperative, three months postoperative and six months postoperative
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