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Clinical Trials/NCT01570114
NCT01570114
Completed
Not Applicable

EFFICACY OF A SELF EXPANDABLE FULLY COVERED METALLIC STENT IN THE TREATMENT OF BENIGN COLONIC STRICTURES

Société Française d'Endoscopie Digestive0 sites43 target enrollmentJanuary 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Colonic Diseases
Sponsor
Société Française d'Endoscopie Digestive
Enrollment
43
Primary Endpoint
Symptom resolution of colonic occlusion
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

Self-expanding metallic stent placement is a safe and effective endoscopic procedure increasingly used to relieve colonic obstruction. Fully covered metal stents (FCSEMS) and plastic stents have been recently developed to reduce both hyperplastic (non tumoral) and tumoral tissue ingrowth. These fully covered metal or plastic stents have several advantages over non-covered stents, including the possibility of retrieval and limited local tissue reaction, while providing alleviation of obstruction at possibly lower costs. Only few reports of fully covered metal stent placement in patients with benign colorectal strictures are available in the literature. The aim of this study was to assess the effectiveness of FCSEMS in the management of the colonic benign strictures.

Detailed Description

It is a national multicentric retrospective study on the use of fully covered metal stent placement in patients with benign colorectal strictures. Consecutive patients above 18 years of age with a symptomatic benign colonic stricture despite optimal medical and/or endoscopic dilation therapy and which required the use of a FCSEMS were included. All strictures were confirmed to be benign by histology. All details concerning previous history, origins and treatment (medical or endoscopic) of the colonic stenosis were collected from the medical file. Senior endoscopists with an experience of more than 50 colonic stent placements performed the procedure under general propofol-induced anesthesia with the same technic (The stent was placed under fluoroscopic and videoendoscopic controls). Patients were required after the procedure to take oral osmotic laxatives regularly. Post-stenting complications were defined as immediate (during the procedure), early (occurring ≤ 30 days) and late (\> 30 days) after the procedure. Stent removal and routine follow up endoscopy were scheduled 4 to 6 weeks after placement in most patients or earlier if complications occurred. All patients were followed up at regular intervals based on their clinical situation. A retrospective chart review was performed to analyze the long-term outcome of the patients.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
October 2011
Last Updated
14 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Société Française d'Endoscopie Digestive
Responsible Party
Principal Investigator
Principal Investigator

VANBIERVLIET

Medical doctor - study coordinator and director of the endoscopy unit in universitary hospital of Nice (France)

Société Française d'Endoscopie Digestive

Eligibility Criteria

Inclusion Criteria

  • patients above 18 years of age
  • symptomatic benign colonic stricture despite optimal medical and/or endoscopic dilation therapy

Exclusion Criteria

  • Previous insertion or treatment of the stricture with metallic (covered or uncovered) stent

Outcomes

Primary Outcomes

Symptom resolution of colonic occlusion

Time Frame: 48 hours

Defined as the clinical (stools, stop pain) and radiological evidence of colonic decompression within 48 hours of stent insertion and without the need for reintervention

Secondary Outcomes

  • Successful stent placement(Immediatly after stent insertion (one minute))
  • Successful stent retrieval(One minute (during colonoscopy for stent retrieval))
  • Occurrence of any complication during interventional endoscopy, stent retrieval and the follow-up(60 days)
  • Recurrence of colonic occlusion(60 days, 6 months and one year)

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