The differences of clinical outcome of brace and non-brace usage after arthroscopic anterior cruciate ligament reconstruction with hamstring tendon graft: A randomized controlled trial
Phase 1
Recruiting
- Conditions
- Patients who diagnosed as having primary ACL injury (from physical examination by orthopedist or positive finding of MRI knee)ACL injury,ACLR,Hamstring graft
- Registration Number
- TCTR20200503004
- Lead Sponsor
- /A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 118
Inclusion Criteria
1. Patients who diagnosed as having primary ACL injury (from physical examination by the orthopedist or r positive finding of MRI knee)
2. Aged from 18 to 50 years
3.Ability to comply with a rehabilitation program
4.Ability to cooperate with the interviewers
Exclusion Criteria
1.Meniscal repair
2.Previous either knee surgery
3.Concomitant PCL, MCL or LCL injury with the requiring surgery
4.Chondral lesions requiring other procedures such as microfracture, osteochondroplasty or osteochondral allograft transplantation (except debridement)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Functional knee score time zero, 8 weeks, 3 months and 6 months Lysholm and Tegner score, interview by research assistance
- Secondary Outcome Measures
Name Time Method Quadriceps strength time zero, 8 weeks, 3 months and 6 months Contrex MJ Multijoint module 2018,Pain score time zero, 8 weeks, 3 months and 6 months VAS pain scale,Stability test time zero, 8 weeks, 3 months and 6 months Ligament Arthrometer