Actively Recruiting
Hybrid Endoscopic Stricturotomy Plus Balloon Dilation Versus Stricturotomy Alone for Short Crohn's Disease Strictures
Led by Asian Institute of Gastroenterology, India · Updated on 2025-07-17
40
Participants Needed
1
Research Sites
106 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Crohn's disease is a chronic condition that can lead to inflammation and narrowing (strictures) of the intestine, causing symptoms like pain, bloating, and difficulty with bowel movements. These strictures are often treated with endoscopic procedures such as balloon dilation or stricturotomy to widen the narrowed segments and relieve symptoms. The HEIST Study is a randomized clinical trial designed to compare two endoscopic treatment strategies for short Crohn's disease-related strictures (less than 3 centimeters in length). One group will undergo endoscopic stricturotomy alone, while the other group will receive a combination of stricturotomy followed by balloon dilation (hybrid approach). The goal is to determine whether the hybrid approach improves long-term outcomes such as symptom relief, reduced need for repeat procedures, and avoidance of surgery. Patients will be followed for 12 months after treatment to assess durability of response, quality of life, and any complications or additional interventions needed. This study aims to provide high-quality evidence to guide endoscopic treatment of intestinal strictures in Crohn's disease and to help identify the most effective and safest approach for long-term symptom control.
CONDITIONS
Official Title
Hybrid Endoscopic Stricturotomy Plus Balloon Dilation Versus Stricturotomy Alone for Short Crohn's Disease Strictures
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 65 years
- Diagnosed Crohn's disease based on clinical, endoscopic, histologic, or radiologic criteria
- Presence of fibrotic or mixed strictures measuring less than 3 cm in length
- A maximum of two strictures per patient
- Strictures located in endoscopically accessible sites
You will not qualify if you...
- Predominantly ulcerated or active inflammatory strictures
- Strictures longer than 3 cm
- Strictures not accessible via standard colonoscopy
- Pregnancy
- Three or more strictures identified in a single patient
- Prior endoscopic stricturotomy at the same stricture site
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Asian Institute of Gastroenterology
Hyderabad, Telangana, India, 500082
Actively Recruiting
Research Team
P
Partha Pal, MD, DNB, MRCP (UK), FASGE
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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