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Clinical Trial Details — Status: No longer available

Administrative data

NCT number NCT02564224
Other study ID # CRCCZ-S01
Secondary ID
Status No longer available
Phase
First received
Last updated

Study information

Verified date June 2018
Source Zhejiang University
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

Temporary stomas has been performed to reduce complications after colorectal cancer surgery, especially in high-risk anastomosis. Different closure technics showed different outcome. The aim of this study is to compare the scar length , surgical site infection and pain score of purse-string wound closure vs conventional closure.


Recruitment information / eligibility

Status No longer available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Receiving temporary ostomy because of colorectal cancer at least 3 months ago;

- Age of=18 and =80

Exclusion Criteria:

- Not willing or incapable to comply with all study visits and assessments

- Evidence of any other disease, metabolic dysfunction, physical examination finding or laboratory finding giving reasonable suspicion of a disease or condition that puts the patient at high risk for treatment-related complications

Study Design


Intervention

Procedure:
Pursestring Wound Closure
Procedure: Pursestring Wound Closure
Conventional Wound Closure
Procedure: Conventional Wound Closure
Device:
prolene


Locations

Country Name City State
China Second Affiliated Hospital Zhejiang University College of Medicine Hangzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Zhejiang University

Country where clinical trial is conducted

China, 

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