Endoscopically Placed Lumen-Apposing Metal Stents for the Treatment of Symptomatic Intestinal Strictures in Individuals With Inflammatory Bowel Disease

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorOttawa Hospital Research Institute

About this trial

This is a single-center prospective pilot study in patients with symptomatic partially obstructing intestinal strictures without severe active inflammation or penetrating complications, evaluating the use of LAMS with respect to symptom and quality of life improvement and the development of stent-related complications.

Eligibility criteria

Qualifiers

≥18 years of age

Established Diagnosis of inflammatory bowel disease

Symptomatic, single, fibrostenotic or anastomotic stricture <6 cm in length without severe active inflammation, pre-stenotic intestinal fistula or penetrating complication, and within reach of the adult colonoscope (colon or terminal ileum)

Ability to accurately gauge stricture length with imaging and safely deploy the stent using conventional fluoroscopic techniques

Disqualifiers

More than one intestinal stricture

Stricture out of reach of standard adult colonoscope

High-grade stricture (complete or near complete bowel obstruction

Severe active inflammation in the stricture or associated penetrating complication, including fistula, inflammatory phlegmon or abscess

Trial design

Treatments tested in this trial

  • Endoscopically placed lumen-apposing metal stents for the treatment of IBD-strictures

Treatment groups

20 Participants
are divided into 1 treatment group

Locations

This trial has no locations