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Clinical Trials/NCT03053232
NCT03053232
Unknown
Not Applicable

Purse String Suture Device Versus Endoclip in the Treatment of Immediate Endoscopic Procedure Associated Gastrointestinal Perforation

Affiliated Hospital to Academy of Military Medical Sciences1 site in 1 country100 target enrollmentFebruary 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intervention
Sponsor
Affiliated Hospital to Academy of Military Medical Sciences
Enrollment
100
Locations
1
Primary Endpoint
Technique success rate
Last Updated
9 years ago

Overview

Brief Summary

Nowadays, endoscopic techniques have been applied for diagnosing and treating a variety of gastrointestinal diseases, such as endoscopic submucosal dissection (ESD) and endoscopic mucosal resection (EMR)technique for removing early gastrointestinal mucosal cancers. Endoscopic procedure associated gastrointestinal perforation is one of the the most severe complications, which is associated with high morality and needs timely detection and effective treatment in clinical practice.Over 90% procedure associated gastrointestinal perforation occurs immediately within 24 h after endoscopic procedure.Endoclips have been widely used in closing the immediate gastrointestinal perforations, but the location of the endoclips could influence the effective rate, limiting its application. In addition, multiple endoclips should be placed under endoscopy for a relatively large perforation, which could increase the medical cost and the procedure time. At recent, a new purse string suture device (LeoMed, China) has been developed by us and introduced to the clinicalmanagement of such patients with procedure associated gastrointestinal perforations. Clinical data validated that the usage of this new purse string suture in treating immediate procedure associated perforations was greatly convenient and effective with very low reoperation rate and postoperative complication rate. A specially designed loop was equipped in this device, which could be tightened under endoscopy. Thus, compared with the placement of endoclips, this device could be more convenient and effective in completely closing the gastrointestinal perforations.This study will test whether purse string suture device will increase the effectiveness of closingimmediate procedure associated gastrointestinal perforationsunder endoscopyin a randomized controlled trialby comparing the use of purse string suture deviceand endoclips.

Detailed Description

This is a randomized controlled trial comparing the use of purse string suture device versus endoclips for closing procedure associated gastrointestinal perforation under endoscopy, which is one of the most severe complications and needs timely treatment. Endoclips have been widely used in closing the gastrointestinal perforations, but the location of the endoclips could significantly influence the effective rate. In addition, multiple endoclips will be needed for a relatively large perforation, which could increase the medical cost and the procedure time. At recent, a new purse string suture device has been developed and introduced to the clinicalmanagement of such patients with gastrointestinal perforations. A loop was equipped in this device, which could be tightened. Thus, compared with endoclips, this device could be more convenient and effective in completely closing the gastrointestinal perforations. This study will test whether purse string suture device will increase the effectiveness of treating procedure associated gastrointestinal perforations under endoscopy in a randomized controlled trial.

Registry
clinicaltrials.gov
Start Date
February 1, 2017
End Date
January 2018
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Affiliated Hospital to Academy of Military Medical Sciences
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients ≥18 Years
  • Immediate procedure associated gastrointestinal perforation (i.e. post-ESD perforation, post-EMR perforation;complications of endoscopic examination and procedure)
  • American Society of Anesthesiology risk class 1, 2 or 3

Exclusion Criteria

  • Patients \<18 years
  • Patients with thrombocytopenia (platelet count \< 50,000/microL) or elevated - International Normalized Ratio (INR \> 1.5)
  • Hemodynamic instability
  • Pregnancy and lactation
  • Patients who are unable or unwilling to give an informed consent
  • Chronic fistula following abdominal surgery
  • Pyriform fossa perforation

Outcomes

Primary Outcomes

Technique success rate

Time Frame: 1 year

Percentage of patients who successfully receive endoscopical interventions

Secondary Outcomes

  • Medical cost(1 year)
  • Operation time(1 year)
  • Effective rate(1 year)
  • Reoperation rate(1 year)
  • Postoperative pain(1 year)
  • Postoperative complication rate(1 year)
  • Postoperative hospitalization(1 year)
  • Time to resume diet(1 year)

Study Sites (1)

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