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collagen sponge clincal research

Collagen sponge

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17010599
Enrollment
Unknown
Registered
2017-02-09
Start date
2017-02-20
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemostasis after general surgery

Interventions

controlled group:Wuxi beidi collagen sponge
experiment group:Hebei Collagen collagen sponge

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Male or female aged 18 to 75 years; 2. general surgery patients with surgical wound hemostatic surgery; 3. patients without active bleeding; 4. to understand the purpose of the test, voluntary participation and signing of informed consent; 5. willing to follow the test.

Exclusion criteria

Exclusion criteria: 1. surgical group iii incision operation; 2. emergency operation; 3. platelet count is less than 50 ×10^9/l; 4. the prothrombin time pt = 18 s; 5. allergy for the study material; 6. HIV and syphilis patients; 7. difficult to make exact evaluation of the efficacy and safety of the instrument; 8. other hemostatic materials used during operation such as gelatin sponge, cellulose type material, fibrin glue, etc. 9. the researchers judged patients with poor compliance, unable to complete the study as required; 10. poor compliance for follow-up; 11. researchers condered person not suitable for the clinical trial.

Design outcomes

Primary

MeasureTime frame
Success of hemostasia in 5 minute;Success of hemostasia in 3 minute;

Countries

China

Contacts

Public ContactZheng Qi

Shanghai Sixth People's hospital

zhengqi1957@yeah.net+86 18930177886

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026