Clinical study for the method of transosseous suture compared suture anchor in the minimally invasive rotator cuff repair
- Conditions
- ROTATOR CUFF TEAR
- Registration Number
- ITMCTR1900002380
- Lead Sponsor
- Wangjing Hospital, China Academy of Chinese Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
1. Aged between 50 and 80 years;
2. Full-thickness rotator cuff lesion (Tearing of supraspinatus or combined infraspinatus);
3. First operation in this side shoulder;
4. The width of rotator cuff tear measured under arthroscope ranged from 15 mm to 40 mm in large nodules;
5. Body mass index =33;
6. BMD measurements were greater than - 2.5 and there was no cystic degeneration of bone or cystic degeneration less than or equal to 1 cm in the area of large nodules;
7. Informed consent to participate in the study.
1) Obvious stiff shoulder (Score of shoulder range of motion shown in this study is less than 60 points);
2) Injuries of the subscapularis tendon;
3) Need for tenodisis of the long head of the biceps;
4) Massive retracted rotator cuff lession(Tear range larger than 4cm);
5) There were cystic lesions larger than 1 cm in diameter or BMD was less than - 2.5;
6) History of ipsilateral shoulder surgery;
7) Other shoulder diseases, such as osteonecrosis, fracture, osteoarthritis (glenohumeral or acromioclavicular joints), Calcific tendinitis;
8) Osteomyelitis, joint infection, sepsis;
9) Muscle atrophy or peripheral nerve injury.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sugaya Class in MRI;
- Secondary Outcome Measures
Name Time Method Shoulder range of motion;Visual analogue scales;Constant-Murley Scales;Shoulder MRI;Safety evaluation;Ultrasonography of shoulder;Health Economic Assessment;