Functional outcome comparison following arthroscopic biceps soft tissue tenodesis with pectoralis major attachment and biceps tenotomy: a randomized controlled trial study
Phase 4
Completed
- Conditions
- ong head of biceps tendon pathologyLong head of biceps tendon
- Registration Number
- TCTR20240515004
- Lead Sponsor
- Bhumibol Adulyadej Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 18
Inclusion Criteria
1.Patient who has LHB Pathology which requiring Arthroscopic rotator cuff repair
2.Patients can make their own decisions about participating in the research
3.Able to read, write and listen to Thai language
4.Age between 40 to 80 years old
5.There is no disease or condition that may obstruct the function of the shoulder, such as severe joint disease that affects walking, neurological disease that affects the function of the shoulder.
Exclusion Criteria
1.Patients suspected of sepsis in any part of the body
2.There is a skin lesion in surgical area.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Functional outcome 12 months Use inferential statistic
- Secondary Outcome Measures
Name Time Method differences of operative time, postoperative pain and complication 12 months Use descriptive statistic