A prospective study to analyse functional outcome, Donor site morbitity and complications in hamstring tendon autograft for anterior cruciate ligament reconstruction in a tertiary care centre
概览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- DEPARTMENT OF ORTHOPAEDICS
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- To assess the functional outcome and donor site morbidity of arthroscopic anterior cruciate ligament reconstruction with hamstring tendon autograft.
概览
简要总结
The most common significant ligamentous injury to the knee joint is an anterior cruciate ligament tear. Recurrent injuries have a higher risk of intra-articular damage, particularly to the meniscus. The ACL reconstruction aims to restore knee stability, allow the patient to return to regular activities, including sports, and delay the onset of osteoarthritis. The choice of graft plays a vital role and the most popular autograft for reconstruction is the hamstring tendon graft.
The aim of this study is to assess the functional outcome and donor site morbidity and analyse complications.
A total of 30 patients who fulfill the criteria will be included and observed prospectively for a period of 6 months. Functional scores will be recorded preoperatively and 6 months after surgery. Donor site morbidities will be assessed with MRC grading for hamstring- flexion at knee and extension at hip.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Symptomatic anterior cruciate ligament insufficiency associated with or without meniscal or chondral injury.
- •MRI evidence of anterior cruciate ligament tear.
- •Examination under anaesthesia showing evidence of anterior cruciate ligament insufficiency like Lachman test and pivot shift test positive.
排除标准
- •Dislocated knee joint.
- •Grade 3 collateral ligament insufficiency.
- •Multi ligamentous injury.
- •Neurovascular insufficiency of affected limb.
结局指标
主要结局
To assess the functional outcome and donor site morbidity of arthroscopic anterior cruciate ligament reconstruction with hamstring tendon autograft.
时间窗: At 4 weeks, At 8 weeks and At 12 weeks
To analyse complications in above mentioned procedure.
时间窗: At 4 weeks, At 8 weeks and At 12 weeks
次要结局
- To analyse complications in above mentioned procedure.(At 4 weeks, At 8 weeks & At 12 weeks)
研究者
DR SHARATHGOWDA KN
SAPTHAGIRI INSTITUTE OF MEDICAL SCIENCES AND RESEARCH CENTRE