CHU de Nantes
Nantes, 44093, France
NCT Number: NCT05584228
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.
Trial opening soon.
Get Notified18 year–70 year
All sexes
Interventional
Not applicable
Nantes, 44093, France
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Combination therapy using 2-2.5 mg/kg oral azathioprine plus subcutaneous infliximab
Other names: Imurel, Remsima
Ileocolonic or small bowel resection
Time frame: 12 months
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
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: 6 months
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: 1, 3, 6, 9, 12, 18 and 24 months
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
Mean total score of CDAI (CROHN'S DISEASE ACTIVITY INDEX ) Scale from 0 to 1100. 0 is the best outcome.
Time frame: 1, 6, 12, 18 and 24 months
Mean values of fecal calprotectin
Time frame: 1, 6, 12, 18 and 24 months
Mean values of CRP
Time frame: 12 months
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 and 24 months
Proportion of patients without any treatment failures
Time frame: 1, 3, 6, 9, 12, 18 and 24 months
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
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
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
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
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
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: 24 months
Number of screened patients refusing to be included
Time frame: 24 months
The reason for refusing
Time frame: 24 months
Proportion of patients with intervention (drug or surgery) -related adverse events during the study
Time frame: 24 months
Incremental cost-utility ratio (cost per Quality-Adjusted Life-Years, QALYs) from a collective perspective
Contact information is provided by the study sponsor or research team.
Nantes University Hospital
Other
SyMptomAtic Stricturing Small Bowel CRohn's Disease - Medical Treatment Versus Surgery, a Prospective, Multi-centre, Randomized, Non-inferiority Trial
Acronym: SMART
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05387031
Constriction, Pathologic, Crohn Disease
Beijing, Beijing Municipality, China
View Trial DetailsNCT04803916
Constriction, Pathologic, Crohn Disease
Jerusalem, Israel
View Trial DetailsNCT06516341
Colitis, Colitis, Ulcerative
Milan, Italy
View Trial DetailsNCT07344428
Crohn Disease, Digestive System Diseases
Guangzhou, Guangdong, China
View Trial Details