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

Primary Purpose

Crohn Disease

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Surgery
TTS balloon dilation
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn Disease

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Balloon dilation

    Surgery

    Arm Description

    TTS balloon dilation

    Resection of the fibrostenotic area

    Outcomes

    Primary Outcome Measures

    Surgery-free period in patients with fibrostenotic Crohns disease
    The time to the need for first surgical treatment in following study intervention in each group

    Secondary Outcome Measures

    Full Information

    First Posted
    November 5, 2018
    Last Updated
    November 6, 2018
    Sponsor
    McMaster University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03735355
    Brief Title
    Endoscopic Balloon Dilation vs Surgery to Treat Short Strictures in Fibrostenosing Crohns Disease: An RCT
    Official Title
    Endoscopic Balloon Dilation as Compared to Surgical Management for the Treatment of Short Strictures in Fibrostenosing Crohns Disease: A Randomized Controlled Trial.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    April 1, 2019 (Anticipated)
    Primary Completion Date
    June 30, 2021 (Anticipated)
    Study Completion Date
    February 28, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    McMaster University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    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 Pre-recruitment phase including proposal, IRB approval, staff training, budget transfer - 9 months Recruitment of patients: 2 years Follow up: 2 years 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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Crohn Disease

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    40 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Balloon dilation
    Arm Type
    Experimental
    Arm Description
    TTS balloon dilation
    Arm Title
    Surgery
    Arm Type
    Active Comparator
    Arm Description
    Resection of the fibrostenotic area
    Intervention Type
    Procedure
    Intervention Name(s)
    Surgery
    Intervention Description
    Surgical resection of fibrostenotic area
    Intervention Type
    Procedure
    Intervention Name(s)
    TTS balloon dilation
    Intervention Description
    Dilation of a stricture using TTS balloon
    Primary Outcome Measure Information:
    Title
    Surgery-free period in patients with fibrostenotic Crohns disease
    Description
    The time to the need for first surgical treatment in following study intervention in each group
    Time Frame
    2 years

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    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

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    26928961
    Citation
    Rieder F, Latella G, Magro F, Yuksel ES, Higgins PD, Di Sabatino A, de Bruyn JR, Rimola J, Brito J, Bettenworth D, van Assche G, Bemelman W, d'Hoore A, Pellino G, Dignass AU. European Crohn's and Colitis Organisation Topical Review on Prediction, Diagnosis and Management of Fibrostenosing Crohn's Disease. J Crohns Colitis. 2016 Aug;10(8):873-85. doi: 10.1093/ecco-jcc/jjw055. Epub 2016 Feb 29.
    Results Reference
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    Endoscopic Balloon Dilation vs Surgery to Treat Short Strictures in Fibrostenosing Crohns Disease: An RCT

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