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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ChiCTR
Last refreshed on: 18 April 2017
Main ID:  ChiCTR-IOR-15006439
Date of registration: 2015-05-24
Prospective Registration: Yes
Primary sponsor: Traumatology Department of The Third Affiliated Hospital of Third Military Medical University
Public title: Prevention Surgical Site Infection With Using Negative Pressure Wound Thearapy In Abdominal Incision
Scientific title: Prevention Surgical Site Infection With Using Negative Pressure Wound Thearapy In Abdominal Incision: A Prospective Random Control Study
Date of first enrolment: 2015-05-30
Target sample size: Experimental group:50;Control:50;
Recruitment status: Pending
URL:  http://www.chictr.org.cn/showproj.aspx?proj=11034
Study type:  Interventional study
Study design:  Randomized parallel controlled trial  
Phase:  Other
Countries of recruitment
China
Contacts
Name: Zhang Lianyang   
Address:  10 Changjiang Zhilu, Daping, Chongqing, China 400042
Telephone: +86 13508308400
Email: hpzhangly@163.com
Affiliation: 
Name: Li Peiyuan   
Address:  10 Changjiang Zhilu, Daping, Chongqing, China 400042
Telephone: +86 15905073485
Email: lpylja@163.com
Affiliation:  The Third Affiliated Hospital of Third Military Medical University
Key inclusion & exclusion criteria
Inclusion criteria: over 18 years old,patient or family members signed informed consent, high-risk patients: including abdominal surgery for malignancy, colorectal, abdominal wall reconstruction
Exclusion criteria: younger than 18 years old,patients who have infected, patients who refuse to participate, negative pressure device allegy

Age minimum: 18
Age maximum: 90
Gender: Both
Health Condition(s) or Problem(s) studied
Surgical Site Infection in Abdominal Incision
Intervention(s)
Experimental group:Negative pressure wound thearapy;Control:Routine approach;
Primary Outcome(s)
the rate of surgical site infection;
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
research fund
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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