Skip to content

To evaluate effects of using peroneus longus tendon graft for ligament reconstruction (anterior cruciate ligament) of knee

Evaluation of changes in biomechanical, clinical and functional outcome of donor ankle following ACL reconstruction with peroneus longus tendon autograft. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/090642
Enrollment
30
Registered
2025-07-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: S00-T88- Injury, poisoning and certain other consequences of external causes

Interventions

Intervention1: Nil: Nil

Sponsors

Elandevan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients with anterior cruciate ligament injury with or without meniscal tears who will require ACL reconstruction. 2) Patients who are above 18 years of age.

Exclusion criteria

Exclusion criteria: 1) Preexisting ankle injury or ankle instability. 2) Patients with osteoarthritis of ankle. 3) Patients with inflammatory arthritis like Rheumatoid arthritis, Gout 4) Patients who require revision anterior cruciate ligament reconstruction 5) Patients with multiligamentous injury of the knee

Design outcomes

Primary

MeasureTime frame
To evaluate changes in the ankle stability of donor ankle using gait analysis and foot pressure analysis in comparison with the contralateral ankle joint.This study will assess the outcome of ankle and foot instability, knee functional outcome and donor site pain following peroneus longus autograft for ACL reconstruction. This study will shed light on whether peroneus longus autograft can be recommended as a primary graft option for ACL reconstruction. Timepoint: outcomes will be assessed at post surgery 6 weeks, 3 momths and 6 months

Secondary

MeasureTime frame
1. To evaluate the changes in functional outcome of the foot & ankle using the AOFAS score & FADI index. 2. To evaluate changes in functional outcome of the knee using Tegner Lysholm score 3. To evaluate the pain at the donor site using the VAS score Timepoint: outcomes will be assessed post surgery at 6 weeks, 3 months & at 6 months

Countries

India

Contacts

Public ContactDr Vineet Thomas Abraham

AIIMS Mangalagiri

elandevangunasekaran@gmail.com8667221057

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026