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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05815355
Other study ID # E2016008
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 2013
Est. completion date September 2015

Study information

Verified date April 2023
Source Sixth Affiliated Hospital, Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date September 2015
Est. primary completion date September 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
exclusive enteral nutrition treatment group


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sixth Affiliated Hospital, Sun Yat-sen University

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical remission after 12 weeks EEN The Crohn's disease activity index (CDAI)<150 was taken as achieving clinical remission. July 2013 to October 2015
Primary Mucosal healing after EEN Mucosal healing was assessed under endoscopy with SES-CD. July 2013 to October 2015
Secondary The high sensitivity C-reactive protein (mg/L) -Inflammatory parameter assessment The high sensitivity C-reactive protein (mg/L) was evaluated at baseline, week 4 and week 12. baseline, week 4 and week 12
Secondary Inflammatory parameter assessment The platelet (10*9/L) was evaluated at baseline, week 4 and week 12. baseline, week 4 and week 12
Secondary The body mass nutritional parameter assessment The body mass was evaluated at baseline, week 4 and week 12. baseline, week 4 and week 12
Secondary The albumin (g/L)- nutritional parameter assessment The albumin (g/L) was evaluated at baseline, week 4 and week 12. baseline, week 4 and week 12
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