Pursestring Wound Closure vs "Gunsight" Skin Incision and Closure Technique to Reverse Stoma

NCT02053948 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 143

Last updated 2019-09-10

No results posted yet for this study

Summary

The use of temporary stomas has been demonstrated to reduce septic complications after colorectal cancer surgery, especially in high-risk anastomosis; therefore, it is necessary to reduce the number of complications secondary to ostomy takedowns, namely wound infection. The aim of this study is to compare the rates of superficial wound infection, healing time and patient satisfaction after pursestring closure vs "gunsight" skin incision and closure technique closure.

Conditions

  • Colostomy

Interventions

PROCEDURE

Pursestring Wound Closure

PROCEDURE

Gunsight Skin Incision and Closure Technique

Sponsors & Collaborators

  • Beijing Friendship Hospital

    collaborator OTHER
  • Shengjing Hospital

    collaborator OTHER
  • Hebei Medical University Fourth Hospital

    collaborator OTHER
  • Sixth Affiliated Hospital, Sun Yat-sen University

    collaborator OTHER
  • Peking University People's Hospital

    collaborator OTHER
  • Peking Union Medical College Hospital

    collaborator OTHER
  • Chinese PLA General Hospital

    collaborator OTHER
  • Jinling Hospital, China

    collaborator OTHER
  • Cancer Institute and Hospital, Chinese Academy of Medical Sciences

    collaborator OTHER
  • First Hospital of China Medical University

    collaborator OTHER
  • Beijing Chao Yang Hospital

    lead OTHER

Principal Investigators

  • Jiagang Han, Professor · Beijing Chao Yang Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2017-12-30
Completion
2017-12-30

Countries

  • China

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02053948 on ClinicalTrials.gov