A study to compare outcomes after ACL surger

Anterior Cruciate Ligament Reconstruction Using Peroneus Autograft Augmented with or without dehydrated Human Amnion/ Chorion Membrane Allograft: A prospective double-blinded randomized comparative study - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/12/098913

Enrollment

Registered

2025-12-11

Start date

Unknown

Completion date

Unknown

Last updated

2026-01-12

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Peroneus longus tendon autograft with dehydrated amnion chorion membrane augmentation: Arthroscopic ACL reconstruction using peroneus longus tendon autograft augmented with dehydrated a

postoperative functional and clinico-radiological outcomes assessed at 9 months. Control Intervention1: Peroneus longus tendon autograft without augmentation: Arthroscopic ACL reconstruction using per

postoperative functional and clinico-radiological outcomes assessed at 9 months.

Eligibility

Inclusion criteria

Inclusion criteria: 18 - 60 years irrespective of gender

Exclusion criteria

Exclusion criteria: Multi ligament injury Open wounds Fractures

Design outcomes

Primary

Measure	Time frame
To compare clinicoradiographic outcomes by following scores vas IKDC Tegner Lysholm Timepoint: 9 months	—

Secondary

Measure	Time frame
Graft rejection Retears Infection rateTimepoint: 9 months	—

Countries

India

Contacts

Public ContactDr Vilash Raj Singh

Post Graduate institute of medical education and research, chandigarh

himanshu.bhayana.mamc@gmail.com9599149380

Outcome results

None listed

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