A clinical trial to study differences in result of two key hole techniques of knee ligament reconstruction using two different graft materials.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: S835- Sprain of cruciate ligament of knee
- Registration Number
- CTRI/2022/06/043039
- Lead Sponsor
- Dr Samir Chandrakant Dwidmuthe
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Outcome: <br/ ><br>To compare the short-term functional outcome of single-bundle ACL reconstruction using Peroneus Longus graft and hamstring graft. <br/ ><br>Timepoint: 2 weeks, 6 weeks, 3 months, 6 months <br/ ><br>
- Secondary Outcome Measures
Name Time Method Secondary Outcomes: <br/ ><br>a)To evaluate the donor site morbidity after PL tendon harvest. <br/ ><br>b)To compare the changes in thigh circumference in both groups of patients.Timepoint: 2 weeks, 6 weeks, 3 months, 6 months