๐ฌIn plain words
What the trial is, and whether it could suit you
The goal of this observational study is to evaluate the effectiveness and safety of exclusive enteral nutrition (EEN) in adults with active Crohn's disease (CD), particularly in patients with complicated disease such as stricturing disease, enteric fistula, and intra-abdominal abscess. The main questions it aims to answer are:
* What is the clinical remission rate at Week 12 in adults with active CD treated with EEN?
* How does EEN affect clinical response, endoscopic outcomes, inflammatory markers, nutritional status, BMI, and safety during follow-up?
Participants will:
* start EEN at baseline and be followed through Week 12;
* receive EEN as the main treatment approach during the study period;
* complete clinical, laboratory, nutritional, and safety assessments at prespecified follow-up visits;
* undergo endoscopic assessment when endoscopy is performed as part of routine care; and
Sign in to get the eligibility rules as simple questions to take to your doctor.
๐ Eligibility rules (as published)
Inclusion Criteria:
1. Age โฅ18 years.
2. Diagnosis of Crohn's disease established on the basis of overall clinical assessment, including compatible clinical history and standard endoscopic, histologic, and/or radiologic findings, as determined by the treating physician. Histologic confirmation at baseline is not required if endoscopy or biopsy is not feasible or clinically inappropriate because of severe disease, poor nutritional status, or intra-abdominal abscess/sepsis.
3. Active Crohn's disease at baseline, as determined by the treating physician.
4. Willingness to initiate and receive exclusive enteral nutrition (EEN) as the sole induction therapy as part of physician-directed routine care.
5. Presence of malnutrition or nutritional risk and clinical indication for EEN.
6. Patients with intestinal complications, including enteric fistula, intestinal stricture, and/or intra-abdominal abscess, are eligible if considered appropriate for EEN-based management by the treating physician.
7. Ability and willingness to provide written informed consent and to comply with study assessments and follow-up for 12 weeks.
Optional clarifying note:
In participants without histologic confirmation at baseline, the diagnosis may be further confirmed during follow-up when clinically feasible, including by endoscopic biopsy or surgical pathology.
Exclusion Criteria
1. Any absolute contraindication to enteral nutrition, including but not limited to gastrointestinal perforation, uncontrolled gastrointestinal bleeding, severe hemodynamic instability/shock, or other conditions where enteral feeding is not clinically appropriate.
2. Immediate need for emergency surgery at baseline.
3. Inability or unwillingness to receive EEN as the sole induction therapy at baseline.
4. Any condition that, in the investigator's opinion, would make participation unsafe or would substantially interfere with study assessments or follow-up.
๐
What it tests
- Exclusive Enteral Nutrition
The Sixth Affiliated Hospital, Sun Yat-sen University
Guangzhou, China
๐ค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ always decide together with your own doctor.