Rotator cuff tear
Conditions
Interventions
Experimental group:Allogeneic umbilical cord and conventional surgical therapy (cord anchor)
control group :conventional surgical therapy (cord anchor)
Sponsors
Shanghai Sixth People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Chinese male or female aged 18 or above; 2. The tear pattern was a large tear (rotator cuff tear >=3 cm) . 3. Those who had no pregnancy plan within 6 months after joining the group and took effective contraception voluntarily; 4. Voluntarily sign an informed consent form; 5. Patients with adequate language comprehension who voluntarily completed the entire study in accordance with the Protocol.
Exclusion criteria
Exclusion criteria: 1. Patients with Alzheimer's disease or dementia who are too delirious to make subjective assessments; 2. Participants in another clinical trial (including drug clinical trials) within 6 months; 3. A pregnant, lactating woman; 4. Obvious osteoarthritis of shoulder joint; 5. Combined with humeral fracture; 6. History of shoulder instability. 7. Severe Systemic or local infection; 8. Patients the researchers considered unsuitable for inclusion.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rotator Cuff Healing Grade; | — |
Countries
China
Contacts
Public ContactZhao Jinzhong
Shanghai Sixth People's Hospital
Outcome results
None listed