ChiCTR2000036989已完成Unknown
A randomized controlled trial comparing hamstring and peroneus longus tendon autografts in anterior cruciate ligament reconstruction
AO Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年6月15日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- fucntiona outcome of knee
研究概览
简要总结
- Compare the clinical and functional outcome of Anterior cruciate ligament reconstruction using hamstring auto graft v/s peroneus longus auto graft;
- To assess any problem in foot using Visual analogue scale (VAS) and foot and ankle disability index;
- Compare complications associated with hamstring versus peroneus longus graft.
研究设计
- 研究类型
- Interventional
- 主要目的
- 随机平行对照
- 盲法
- None
入排标准
- 性别
- All
入选标准
- •No other injury except ACL tear;
- •No any previous history of trauma or infection in the foot from where graft will be harvested;
- •Participant is willing and able to give informed consent for participation in the trial;
- •Male or female ages 18-50 years old with complete tear of ACL and symptomatic clinically;
- •Able to complete treatment for the study period.
排除标准
- •Pregnant Women;
- •Patients with any psychiatric issues, impeding the completion of study;
- •Patient not willing for study.
研究组 & 干预措施
Hamstring tendon autograft
Anterior cruciate ligament reconstruction
peronues longus autograft
Anterior cruciate ligament reconstruction
结局指标
主要结局
fucntiona outcome of knee
时间窗: pre-operatvie, 3,6 and 12 months postoperatively
functional outcome of knee
时间窗: pre-operatvie, 3,6 and 12 months postoperatively
foot and ankle disability
时间窗: pre-operatvie, 3,6 and 12 months postoperatively
pain intensity
时间窗: pre-operatvie, 3,6 and 12 months postoperatively
次要结局
- Bleeding
- saphenous nerve damage
研究者
研究点 (1)
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