peri-tendinous adhesion
Conditions
Interventions
The experimental group:Collect samples of adhesive waste tissue
The control group:The tendon at the end of anastomosis was removed
Sponsors
Shanghai Sixth People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18 to 65-year-olds male or female; 2. Preoperative physical examination confirms tendon rupture/adhesion, requiring tendon anastomosis or tendolysis; 3. Good compliance, healthy psychological state, and able to cooperate with experimental observation; 4. Without complications(Diabetes, acute infection, hyperthyroidism, heart failure, hepatitis, nephritis). Fully informed of the purpose, method and possible discomfort of the test, and agree to participate in the test and sign an informed consent form.
Exclusion criteria
Exclusion criteria: 1. Participants in other clinical trials during the last 3 months; 2. There are other serious systemic diseases and organ dysfunction; 3. pregnant women, lactating mothers, or in the near future has a bearing planning that can't take effective contraception measures; 4. apparent dysfunction of liver and kidney patients. The researchers determined that there was anything unsuitable for including.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| TGF-ß1;iNOS, CD11c;CD206, Arg 1; | — |
Secondary
| Measure | Time frame |
|---|---|
| Nestin; | — |
Countries
China
Contacts
Public ContactLiu Shen
Shanghai Sixth People's Hospital
Outcome results
None listed