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A clinical trial to study differences in result of two key hole techniques of knee ligament reconstruction using two different graft materials.

Functional Outcome of Single Bundle Arthroscopic Anterior Cruciate Ligament Reconstruction using Peroneus Longus Graft and Hamstring Graft â?? An Open-Label Randomized Comparative Study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043039
Enrollment
36
Registered
2022-06-06
Start date
Unknown
Completion date
Unknown
Last updated
2022-06-27

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 Health Condition 2: S835- Sprain of cruciate ligament of knee

Interventions

Intervention1: Peroneus Longus graft: Arthroscopic single bundle anterior cruciate ligament reconstruction using Peroneus Longus graft. Approximate time for surgery 2 hrs. Control Intervention1: Hamst

Sponsors

Dr Samir Chandrakant Dwidmuthe
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Patients diagnosed with complete ACL rupture on the basis of clinical examination and MRI findings 2. Age 18 to 45 years

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. Associated other grade 3 knee ligament injuries 2. Grade 4 Chondral injuries ( >1 cm) 3. Patients with associated meniscal injuries requiring meniscal repair 4. Knee arthritic changes 5. Fractures around the knee 6. History of previous knee surgery 7. Pre-existing knee deformities 8. Partial ACL ruptures 9. Foot/Ankle deformity precluding PL tendon harvest

Design outcomes

Primary

MeasureTime frame
Primary Outcome: To compare the short-term functional outcome of single-bundle ACL reconstruction using Peroneus Longus graft and hamstring graft. Timepoint: 2 weeks, 6 weeks, 3 months, 6 months—

Secondary

MeasureTime frame
Secondary Outcomes: a) To evaluate the donor site morbidity after PL tendon harvest. b) To compare the changes in thigh circumference in both groups of patients.Timepoint: 2 weeks, 6 weeks, 3 months, 6 months—

Countries

India

Contacts

Public ContactDr Mainak Roy

All India Institute of Medical Sciences, Nagpur

samirdwidmuthe@aiimsnagpur.edu.in9422904819

Outcome results

None listed

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