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Synbiotic Treatment in Crohn's Disease Patients
This study has been completed.
Study NCT00305409   Information provided by University of Dundee
First Received: March 20, 2006   Last Updated: February 10, 2009   History of Changes
This Tabular View shows the required WHO registration data elements as marked by

March 20, 2006
February 10, 2009
June 2006
Reduction in mucosal TNF-alpha
Same as current
Complete list of historical versions of study NCT00305409 on ClinicalTrials.gov Archive Site
  • Number of patients in remission as assessed by CDAI.
  • Significant differences in mucosal regeneration between pre-synbiotic and post-synbiotic therapy groups and pre-control and post-control therapy groups.
  • Differences in TNF-alpha, IL-18 and INF-gamma between the post-synbiotic and post-control groups.
  • Number of patients in remission as assessed by CDAI.
  • Significant differences in mucosal regeneration between pre-synbiotic and post-synbiotic therapy groups and pre-control and post-control therapy groups.
  • Differences in TNF-alpha, IL-18 and INF-gamma between the post-synbiotic and post-control groups.
 
Synbiotic Treatment in Crohn's Disease Patients
Synbiotic Treatment in Crohn's Disease Patients

The purpose of this study is to determine whether administration of a synbiotic, comprised on inulin and a bifidobacterial probiotic will colonise the gut wall and down-regulate TNF-alpha and other pro-inflammatory cytokines in the mucosa of Crohn's patients with active disease to reduce mucosal inflammation and induce remission.

Crohn's disease is one of the two main forms of idiopathic inflammatory bowel disease. The Th1-mediated inflammatory response in Crohn's disease is characterised by increased IL-18 and INF-gamma and especially TNF-alpha, which are formed by lamina propria mononuclear cells. The aim of this investigation is to determine whether a synbiotic comprised of inulin and a bifidobacterial probiotic, that we have previously shown to down-regulate TNF-alpha and other proinflammatory cytokines in the gut mucosa in ulcerative colitis patients with active disease, can colonise the bowel wall, reduce mucosal inflammation and induce remission in Crohn's disease patients with active disease, in a randomised controlled trial. Crohn's disease is associated with high mortality and incurs significant social, commercial and NHS costs. Many patients are refractile to standard treatments, which often have undesirable side effects. An inexpensive, effective and non-toxic treatment based on the synbiotic concept would contribute greatly to relieving the clinical and financial burdens of the disease.

 
Interventional
Treatment, Randomized, Double-Blind, Placebo Control, Single Group Assignment, Efficacy Study
Crohn's Disease
Drug: Synbiotic (Synergy I / B.longum)
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
50
December 2008
December 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Crohn's disease of large bowel (+/- small bowel disease)
  • 18-79 years old
  • stable doses of medications
  • CDAI >150, <450

Exclusion Criteria:

  • short gut syndrome
  • pregnancy
  • lactation
  • antibiotic therapy in last 3 months
  • probiotic therapy in last 1 month
  • <18, >79 years old
  • CDAI <150 or >450
  • indeterminate colitis, ulcerative colitis
  • alterations to medications in last 3 months
Both
18 Years to 79 Years
No
 
United Kingdom
 
 
NCT00305409
 
RND ID: 2004GA07, LREC Ref: 05/51401/111
University of Dundee
 
Principal Investigator: George MacFarlane, BSc PhD University of Dundee
University of Dundee
February 2009

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.