search
Back to results

Medical Treatment Versus Surgery in Stricturing Small Bowel Crohn's Disease (SMART)

Primary Purpose

Crohn Disease

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Azathioprine + infliximab
Intestinal resection
Sponsored by
Nantes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn Disease focused on measuring Crohn's disease, stricture, resection, infliximab, azathioprine

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age between 18 and 70 years
  • Male or female
  • Documented small bowel CD with intestinal stricture(s) identified on CT, MRI or endoscopy, AND responsible for obstructive symptoms
  • CREOLE score > 2

Exclusion Criteria:

  • Adults under guardianship, safeguard justice or trusteeship
  • Pregnant or breastfeeding female
  • Acute bowel obstruction requiring urgent surgical intervention
  • Suspected or confirmed gastrointestinal perforation
  • Concurrent active perianal sepsis
  • Internal fistulizing disease in association with strictures
  • Colonic stenosis and/or colonic active disease at screening endoscopy
  • Contra-indication to surgery, general anesthesia, anti-TNF, thiopurines
  • Use of corticosteroids (prednisolone > 20 mg daily or equivalent) within 4 weeks prior to visit V0
  • Treatment with any biologics within 8 weeks before visit V0
  • Presence of a stoma
  • HIV/HCV/HBV infection

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Medical treatment

    Surgery

    Arm Description

    Combination therapy with subcutaneous infliximab and azathioprine

    Intestinal resection

    Outcomes

    Primary Outcome Measures

    IBD (inflammatory bowel disease) - related quality of life
    Mean total inflammatory bowel disease questionnaire (IBDQ - Inflammatory Bowel Disease Questionnaire ) score. The total score ranges from 32 to 224, the higher the score the better the quality of life.

    Secondary Outcome Measures

    IBD (inflammatory bowel disease) -related quality of life
    Mean total inflammatory bowel disease questionnaire (IBDQ - Inflammatory Bowel Disease Questionnaire ) score. The total score ranges from 32 to 224, the higher the score the better the quality of life.
    Endoscopic remission
    Proportion of patients achieving endoscopic remission at month 6 (SES-CD < 2 in case of medical treatment or Rutgeerts score < i,2 in case of resection)
    Obstructive symptoms
    Mean total score of CDOS (CROHN'S DISEASE OBSTRUCTIVE SCORE ) Scale frome 0 to 6. 0 is the best outcome.
    Clinical activity
    Mean total score of CDAI (CROHN'S DISEASE ACTIVITY INDEX ) Scale from 0 to 1100. 0 is the best outcome.
    inflammatory biomarkers (fecal calprotectin)
    Mean values of fecal calprotectin
    inflammatory biomarkers ( C-reactive protein [CRP])
    Mean values of CRP
    imaging parameters
    Proportion of patients with an improvement in wall thickening, contrast enhancement, T2-signal increase, diffusion weighted-signal increase and length of pathological segment at month 12 as compared to screening imaging (MRI) by physician global assessment
    treatment failures
    Proportion of patients without any treatment failures
    patient-reported outcomes (disability)
    Mean total score of IBD-DI (INFLAMMATORY BOWEL DISEASE DISABILITY INDEX ) Score from 0 to 100. 0 is the best outcome (no disability)
    patient-reported outcomes (work productivity)
    Mean total score of WPAI (WORK PRODUCTIVITY AND ACTIVITY IMPAIRMENT QUESTIONNAIRE) In percentage from 0 to 100.
    patient-reported outcomes (fatigue)
    Mean total score of FACIT-F (Functional Assessment of Chronic Illness Therapy ) scores from 0 to 52, with higher scores corresponding to less fatigue
    patient-reported outcomes (body image)
    Mean total score of body image questionnaire Ranges from 0 to 30 and can be calculated by summing up the 10 items. A higher score means a higher level of body image disturbance
    patient-reported outcomes (generic quality-of-life)
    Mean total score of SF-36 (QUESTIONNAIRE SHORT FORM 36 HEALTH SURVEY ) Score ranging from 0 to 100. A low score reflects a perception of poor health, loss of function, presence of pain. A high score reflects a perception of good health, absence of functional deficit and pain
    patient-reported outcomes (anxiety/depression)
    Mean total score of HAD (Hospital Anxiety and Depression scale) 14 items rated from 0 to 3. Seven questions relate to anxiety (total A) and seven others to the depressive dimension (total D), thus allowing two scores (maximum score for each score = 21). Minimum : 0. The best outcome is 0.
    Patient's acceptability -patients refusing to be included
    Number of screened patients refusing to be included
    patient's acceptability - The reason
    The reason for refusing
    intervention-related adverse events
    Proportion of patients with intervention (drug or surgery) -related adverse events during the study
    efficiency of medical treatment compared to surgery as assessed by a cost-utility analysis performed from a collective perspective
    Incremental cost-utility ratio (cost per Quality-Adjusted Life-Years, QALYs) from a collective perspective

    Full Information

    First Posted
    September 26, 2022
    Last Updated
    October 14, 2022
    Sponsor
    Nantes University Hospital
    Collaborators
    Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT05584228
    Brief Title
    Medical Treatment Versus Surgery in Stricturing Small Bowel Crohn's Disease
    Acronym
    SMART
    Official Title
    SyMptomAtic Stricturing Small Bowel CRohn's Disease - Medical Treatment Versus Surgery, a Prospective, Multi-centre, Randomized, Non-inferiority Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    April 1, 2023 (Anticipated)
    Primary Completion Date
    October 1, 2027 (Anticipated)
    Study Completion Date
    October 1, 2027 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Nantes University Hospital
    Collaborators
    Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives

    4. Oversight

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

    5. Study Description

    Brief Summary
    The objective of the SMART trial is to compare a combination therapy using azathioprine and subcutaneous infliximab versus ileocecal resection in patients with symptomatic small bowel Crohn's disease.
    Detailed Description
    Crohn's disease (CD) is a chronic, disabling and destructive inflammatory bowel disease (IBD) leading to progressive and cumulative bowel damage, including fistulas and strictures. Strictures are defined as intestinal luminal narrowing and can lead to obstructive symptoms in the medium-to-long term. Symptomatic strictures significantly impair patient's quality of life by the presence of obstructive symptoms such as abdominal pain, nausea, vomiting, abdominal distension, and dietary restrictions leading to malnutrition. Strictures can appear anywhere in the gastrointestinal tract, but affect most commonly the terminal ileum. Epidemiological studies indicate that more than 40% of patients with ileal CD will develop strictures. However, treatment strategies are not well-defined in this indication. Most patients undergo surgery but recent observations indicate that a medical treatment by anti-TNF may be considered in stricturing CD. The European Crohn's Colitis Organization recommends that "ileocecal CD with obstructive symptoms, but no significant evidence of active inflammation, should be treated by surgery". However, the lack of inflammation is difficult to demonstrate and does not predict the extent of fibrosis, and inflammation and fibrosis are often associated. Thus, there is a need for better defining therapeutic strategies. The objective of the SMART trial is to compare for the first time medical versus surgical approaches in stricturing CD. Indeed, up to date, no randomized controlled trial has been conducted to compare medical treatment alone versus surgery in patients with symptomatic stricturing CD. The hypothesis is that medical treatment by a combination therapy using infliximab and azathioprine is non-inferior to surgical resection in terms of health-related quality of life (HRQoL) at 1 year, with the advantage of being conservative as regards the high rates of post-operative recurrence with the subsequent risk of small bowel syndrome, as well as highly more acceptable by patients, especially since infliximab is now available as a biosimilar in a subcutaneous formulation, which should also improve the cost-effectiveness of the medical strategy.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Crohn Disease
    Keywords
    Crohn's disease, stricture, resection, infliximab, azathioprine

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    150 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Medical treatment
    Arm Type
    Experimental
    Arm Description
    Combination therapy with subcutaneous infliximab and azathioprine
    Arm Title
    Surgery
    Arm Type
    Active Comparator
    Arm Description
    Intestinal resection
    Intervention Type
    Drug
    Intervention Name(s)
    Azathioprine + infliximab
    Other Intervention Name(s)
    Imurel, Remsima
    Intervention Description
    Combination therapy using 2-2.5 mg/kg oral azathioprine plus subcutaneous infliximab
    Intervention Type
    Procedure
    Intervention Name(s)
    Intestinal resection
    Intervention Description
    Ileocolonic or small bowel resection
    Primary Outcome Measure Information:
    Title
    IBD (inflammatory bowel disease) - related quality of life
    Description
    Mean total inflammatory bowel disease questionnaire (IBDQ - Inflammatory Bowel Disease Questionnaire ) score. The total score ranges from 32 to 224, the higher the score the better the quality of life.
    Time Frame
    12 months
    Secondary Outcome Measure Information:
    Title
    IBD (inflammatory bowel disease) -related quality of life
    Description
    Mean total inflammatory bowel disease questionnaire (IBDQ - Inflammatory Bowel Disease Questionnaire ) score. The total score ranges from 32 to 224, the higher the score the better the quality of life.
    Time Frame
    1, 3, 6, 9, 18 and 24 months
    Title
    Endoscopic remission
    Description
    Proportion of patients achieving endoscopic remission at month 6 (SES-CD < 2 in case of medical treatment or Rutgeerts score < i,2 in case of resection)
    Time Frame
    6 months
    Title
    Obstructive symptoms
    Description
    Mean total score of CDOS (CROHN'S DISEASE OBSTRUCTIVE SCORE ) Scale frome 0 to 6. 0 is the best outcome.
    Time Frame
    1, 3, 6, 9, 12, 18 and 24 months
    Title
    Clinical activity
    Description
    Mean total score of CDAI (CROHN'S DISEASE ACTIVITY INDEX ) Scale from 0 to 1100. 0 is the best outcome.
    Time Frame
    1, 3, 6, 9, 12, 18 and 24 months
    Title
    inflammatory biomarkers (fecal calprotectin)
    Description
    Mean values of fecal calprotectin
    Time Frame
    1, 6, 12, 18 and 24 months
    Title
    inflammatory biomarkers ( C-reactive protein [CRP])
    Description
    Mean values of CRP
    Time Frame
    1, 6, 12, 18 and 24 months
    Title
    imaging parameters
    Description
    Proportion of patients with an improvement in wall thickening, contrast enhancement, T2-signal increase, diffusion weighted-signal increase and length of pathological segment at month 12 as compared to screening imaging (MRI) by physician global assessment
    Time Frame
    12 months
    Title
    treatment failures
    Description
    Proportion of patients without any treatment failures
    Time Frame
    12 and 24 months
    Title
    patient-reported outcomes (disability)
    Description
    Mean total score of IBD-DI (INFLAMMATORY BOWEL DISEASE DISABILITY INDEX ) Score from 0 to 100. 0 is the best outcome (no disability)
    Time Frame
    1, 3, 6, 9, 12, 18 and 24 months
    Title
    patient-reported outcomes (work productivity)
    Description
    Mean total score of WPAI (WORK PRODUCTIVITY AND ACTIVITY IMPAIRMENT QUESTIONNAIRE) In percentage from 0 to 100.
    Time Frame
    1, 3, 6, 9, 12, 18 and 24 months
    Title
    patient-reported outcomes (fatigue)
    Description
    Mean total score of FACIT-F (Functional Assessment of Chronic Illness Therapy ) scores from 0 to 52, with higher scores corresponding to less fatigue
    Time Frame
    1, 3, 6, 9, 12, 18 and 24 months
    Title
    patient-reported outcomes (body image)
    Description
    Mean total score of body image questionnaire Ranges from 0 to 30 and can be calculated by summing up the 10 items. A higher score means a higher level of body image disturbance
    Time Frame
    1, 3, 6, 9, 12, 18 and 24 months
    Title
    patient-reported outcomes (generic quality-of-life)
    Description
    Mean total score of SF-36 (QUESTIONNAIRE SHORT FORM 36 HEALTH SURVEY ) Score ranging from 0 to 100. A low score reflects a perception of poor health, loss of function, presence of pain. A high score reflects a perception of good health, absence of functional deficit and pain
    Time Frame
    1, 3, 6, 9, 12, 18 and 24 months
    Title
    patient-reported outcomes (anxiety/depression)
    Description
    Mean total score of HAD (Hospital Anxiety and Depression scale) 14 items rated from 0 to 3. Seven questions relate to anxiety (total A) and seven others to the depressive dimension (total D), thus allowing two scores (maximum score for each score = 21). Minimum : 0. The best outcome is 0.
    Time Frame
    1, 3, 6, 9, 12, 18 and 24 months
    Title
    Patient's acceptability -patients refusing to be included
    Description
    Number of screened patients refusing to be included
    Time Frame
    24 months
    Title
    patient's acceptability - The reason
    Description
    The reason for refusing
    Time Frame
    24 months
    Title
    intervention-related adverse events
    Description
    Proportion of patients with intervention (drug or surgery) -related adverse events during the study
    Time Frame
    24 months
    Title
    efficiency of medical treatment compared to surgery as assessed by a cost-utility analysis performed from a collective perspective
    Description
    Incremental cost-utility ratio (cost per Quality-Adjusted Life-Years, QALYs) from a collective perspective
    Time Frame
    24 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age between 18 and 70 years Male or female Documented small bowel CD with intestinal stricture(s) identified on CT, MRI or endoscopy, AND responsible for obstructive symptoms CREOLE score > 2 Exclusion Criteria: Adults under guardianship, safeguard justice or trusteeship Pregnant or breastfeeding female Acute bowel obstruction requiring urgent surgical intervention Suspected or confirmed gastrointestinal perforation Concurrent active perianal sepsis Internal fistulizing disease in association with strictures Colonic stenosis and/or colonic active disease at screening endoscopy Contra-indication to surgery, general anesthesia, anti-TNF, thiopurines Use of corticosteroids (prednisolone > 20 mg daily or equivalent) within 4 weeks prior to visit V0 Treatment with any biologics within 8 weeks before visit V0 Presence of a stoma HIV/HCV/HBV infection
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Catherine Le Berre
    Phone
    (0)2 40 08 31 52
    Ext
    + 33
    Email
    catherine.leberre@chu-nantes.fr

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Medical Treatment Versus Surgery in Stricturing Small Bowel Crohn's Disease

    We'll reach out to this number within 24 hrs