Efficacy of Exclusive Enteral Nutrition in Adult Active Crohn's Disease

Sponsor
Sixth Affiliated Hospital, Sun Yat-sen University (Other)
Overall Status
Completed
CT.gov ID
NCT05815355
Collaborator
(none)
48
26

Study Details

Study Description

Brief Summary

Patients with Crohn's disease (CD) could develop complications such as stricture, intestinal fistula and abdominal abscess. Some CD patients had poor response to medical therapy. The efficacy of exclusive enteral nutrition (EEN) to these adult active CD patients is still unclear. The investigators aim to study the efficacy of EEN in induction of remission in adult active CD patients with complications or poor response to drugs.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: exclusive enteral nutrition treatment group

Detailed Description

Active CD patients following up in our center who had been diagnosed as complicated disease with stricture, intestinal fistula, abdominal abscess and no response to drugs, were recruited since July 2013. Patients were only offered EEN for 12 weeks without using other drugs except that patients with abscess could use antibiotic therapy with or without percutaneous drainage. The disease activity was assessed by the Crohn's disease activity index (CDAI). CDAI<150 was taken as achieving clinical remission. Demographics and clinical variables were recorded. Nutritional (body mass index, albumin) and inflammatory (High sensitivity C-reactive protein and platelet) index were evaluated at baseline, week 4 and week 12. Some patients performed colonoscopy and/or computed tomography enterography (CTE) /resonance enterography(MRE) before and after EEN. Mucosal healing was assessed under endoscopy with SES-CD and the size of abscess was detected by CTE /MRE.

Study Design

Study Type:
Observational
Actual Enrollment :
48 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Efficacy of Exclusive Enteral Nutrition in Adult Active Crohn's Disease With Complications or Failure of Medical Treatment
Study Start Date :
Jul 1, 2013
Actual Primary Completion Date :
Sep 1, 2015
Actual Study Completion Date :
Sep 1, 2015

Outcome Measures

Primary Outcome Measures

  1. Clinical remission after 12 weeks EEN [July 2013 to October 2015]

    The Crohn's disease activity index (CDAI)<150 was taken as achieving clinical remission.

  2. Mucosal healing after EEN [July 2013 to October 2015]

    Mucosal healing was assessed under endoscopy with SES-CD.

Secondary Outcome Measures

  1. The high sensitivity C-reactive protein (mg/L) -Inflammatory parameter assessment [baseline, week 4 and week 12]

    The high sensitivity C-reactive protein (mg/L) was evaluated at baseline, week 4 and week 12.

  2. Inflammatory parameter assessment [baseline, week 4 and week 12]

    The platelet (10*9/L) was evaluated at baseline, week 4 and week 12.

  3. The body mass nutritional parameter assessment [baseline, week 4 and week 12]

    The body mass was evaluated at baseline, week 4 and week 12.

  4. The albumin (g/L)- nutritional parameter assessment [baseline, week 4 and week 12]

    The albumin (g/L) was evaluated at baseline, week 4 and week 12.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. 18 years old

  2. Patients with CD was diagnosed clinically according to previously established international criteria [9]

  3. The diagnosis of stricture, fistula and abdominal abscess was confirmed by ultrasound, CT enterography (CTE), and endoscopy. The bowel stricture should mainly cause by inflammation. Intolerance or failure to steroids or IFX was judged by medical history

  4. The disease was in an active period.

Exclusion Criteria:
  1. Intolerant to EEN or need emergency surgery

  2. The bowel stricture should mainly cause by fibrosis

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Sixth Affiliated Hospital, Sun Yat-sen University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Xiang Peng, Attending physician, Sixth Affiliated Hospital, Sun Yat-sen University
ClinicalTrials.gov Identifier:
NCT05815355
Other Study ID Numbers:
  • E2016008
First Posted:
Apr 18, 2023
Last Update Posted:
Apr 18, 2023
Last Verified:
Apr 1, 2023
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 18, 2023