Double blind, Randomize control trial ; Intraarticular triamcinolone acetone post arthroscopic lysis adhesion prevent recurrent stiffness of the knee.
Phase 4
- Conditions
- Study on knee range of motion and pain score after arthroscopic release of stiff kneeArthroscopic releaseStiff kneeTA injection
- Registration Number
- TCTR20200322005
- Lead Sponsor
- /A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Enrolling by invitation
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
-Patient who was diagnosed as Arthrofibrosis knee and under went arthroscopic lysis adhesion.
Exclusion Criteria
Active infection
Extra-articular course stiff knee
Chronic inflammatory joint disease (RA SLE)
Knee stiffness from tumor
Nerve or spine injury
Previous operative management of stiff knee.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Knee ROM at 1, 6, 12 week post operative at 1, 6, 12 week post operative Range of motion as degree
- Secondary Outcome Measures
Name Time Method VAS at 1, 6, 12 week post operative at 1, 6, 12 week post operative Visual analog score