Skip to content

Endoscopic Balloon Dilation vs Surgery to Treat Short Strictures in Fibrostenosing Crohns Disease: An RCT

Endoscopic Balloon Dilation as Compared to Surgical Management for the Treatment of Short Strictures in Fibrostenosing Crohns Disease: A Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03735355
Enrollment
40
Registered
2018-11-08
Start date
2019-04-01
Completion date
2022-02-28
Last updated
2018-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Crohn Disease

Brief summary

There is currently no standard management to guide the clinicians in treating patients with fibrostenotic disease. European Crohns and Colitis Organization \[ECCO\] recently developed a topical review on prediction, diagnosis and management of fibrostenosing Crohns disease. The review suggests endoscopic balloon dilation, strictureplasty, and intestinal resection as reasonable treatment options for short strictures based on the low grade of evidence.

Detailed description

Study Population All patients with Crohns disease and a short stricture (\<5 cm) within the reach of upper or lower GI endoscopy Study Timeline 1. Pre-recruitment phase including proposal, IRB approval, staff training, budget transfer - 9 months 2. Recruitment of patients: 2 years 3. Follow up: 2 years 4. Analysis and preparing report: 6 months Study Design Single blind randomized controlled trial The data will be blindly analyzed. Double blinding is not possible due to the nature of the study. Study Methods Please see the study flow diagram below. Randomization will be done using computer software generating random numbers. Outcome Measures - A research associate will contact patients on weeks 1,2,4 and months 3,6,12,18 and 24 to record the items mentioned as secondary objectives of the study. \- An interim analysis will be performed after 20 cases complete the study Sample Size 40 patients randomized to two arms undergoing TTS dilation or surgical managements Statistical analysis Comparisons between groups will be done using Student's t-test. Qualitative variables will be summarized as a percentage of the group total and comparisons between groups will be based on the chisquared test. The cumulative relapse rate of each treatment group will be estimated by the Kaplan±Meier method and the difference between treatment groups will be tested by the log rank test. Time to relapse will be compared betweens two groups using a Cox proportional hazards regression analysis. A P value of less than 0.05 is considered to be signicant.

Interventions

PROCEDURETTS balloon dilation

Dilation of a stricture using TTS balloon

PROCEDURESurgery

Surgical resection of fibrostenotic area

Sponsors

McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 40 Patients with Crohns disease and a short stricture (\<5 cm) within the reach of upper or lower GI endoscopy

Exclusion criteria

* Abscess or phlegmon * Fistula * High-grade dysplasia * Malignancy * Previous intervention * Pregnant women

Design outcomes

Primary

MeasureTime frameDescription
Surgery-free period in patients with fibrostenotic Crohns disease2 yearsThe time to the need for first surgical treatment in following study intervention in each group

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026