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
About this trial
This is an interventional treatment trial for Crohn Disease focused on measuring Crohn's disease, stricture, resection, infliximab, azathioprine
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
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
NCT ID
NCT05584228
First Posted
September 26, 2022
Last Updated
October 14, 2022
Sponsor
Nantes University Hospital
Collaborators
Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives
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
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