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Clinical Trials in India / NCT05521867
Active, not recruiting Not applicable

Endoscopic Balloon Dilation Versus Endoscopic Stricturotomy for Short Crohn's Strictures

NCT05521867 · tracked via the Priya Life Science India tracker
Sponsor
Asian Institute of Gastroenterology, India
Phase
Not applicable
Started
2023-02-10
Last updated
2025-07-16

Condition(s) studied

Crohn Disease

Investigational drug(s) / intervention(s)

Endoscopic balloon dilationEndoscopic stricturotomy with or without stricturoplasty

Endoscopic balloon dilation: EBD procedures will be performed with wire guided CRE pneumatic balloon (controlled radial expansion balloon, Boston scientific, Marlborough, MA, USA 0of various sizes based on tightness of the stricture (10-12 mm, 12-15 mm, 15-18 mm, 18-20 mm) with graded dilations with inflation pressures varying from 3-8 ATM pressure. Balloon was inflated for at least 2 minutes and slowly deflated. A maximum of two sessions of dilation will be allowed with a minimum interval of 15-30 days between them.

Endoscopic stricturotomy with or without stricturoplasty: Endoscopic stricturotomy would be done using either a triple-lumen needle-knife (Boston Scientific, Marlborough, MA) or with a electrosurgical IT knife2 (Olympus Medical Systems, Tokyo, Japan) in the setting of endoscopic retrograde cholangiopancreatography (ERCP) Endocut on Erbe medical device (USA Incorporated Surgical Systems, Marietta, GA) with the following electrocautery settings : Endocut Q (effect 3, cut duration 1, cut interval 3). Strictures will be incised in a circumferential or radial fashion until an adequate passage of the scope. Endoclips may be applied post stricturotomy to act as keep treated stricture open and to prevent delayed bleeding (referred as stricturoplasty). Choice of endoclips and decision to perform stricturoplasty would be at the discretion of endoscopist.

Study summary

Crohn's disease (CD) related strictures can be treated endoscopically by endoscopic balloon dilation (EBD) or endoscopic stricturotomy (EST). EBD is is the established endoscopic treatment for short strictures in Crohn's disease. However, roughly half had recurrent symptoms and two third require surgery after EBD. ES have been used initially for endoscopic treatment of patients for whom EBD was unsuccessful. Subsequently it was shown that ES is a better modality for treating CD related strictures (specially short and anastomotic strictures) than EBD lowering the risk of future surgery and procedure related perforation albeit with an increased risk of bleeding. ES was shown to be non-inferior to re-do surgery in chronic pouch anastomotic sinus in ulcerative colitis (UC) and ileocolic anastomotic strictures in CD thus reducing surgical morbidity. However, these two modalities have not been compared in a randomized controlled manner. We aimed to compare the two endoscopic treatments with regard to clinical success, need for surgery or additional endoscopic procedure and safety in patients with CD who have short (\<3 cm), predominantly fibrotic stenosis excluding those in the small bowel not accessible by endoscope/colonoscope.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion criteria Primary confirmed diagnosis of CD with obstructive symptoms 1. Gastro-duodenal and ileo-colonic strictures (both de novo and anastomotic strictures) 2. Short strictures (\<3 cm) 3. Fibrotic or mixed stricture (predominantly fibrotic) 4. Strictures treated with either EST or EBD. Exclusion Criteria: 1. No established diagnosis of CD; 2. No endoscopic therapy; and 3. A combination therapy of EST and EBD at the onset 4. Small bowel CD related stricture requiring enteroscopy guided dilation 5. Predominantly ulcerated strictures (mixed or pure ulcerated strictures) 6. Long strictures (\>3 cm) 7. Pediatric Patients (\<18 years) 8. Pregnant or lactating mother 9. Not willing to participate

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Asian lnstitute of Gastroenterology Hyderabad Telangana

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05521867 on ClinicalTrials.gov ↗ ← All trials in India