Status:

COMPLETED

Rifaximin for the Treatment of Persistent Symptoms in Patients With Celiac Disease

Lead Sponsor:

Columbia University

Collaborating Sponsors:

Bausch Health Americas, Inc.

Conditions:

Celiac Disease

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

Celiac disease is a condition in which the small intestine is damaged by gluten, the storage protein of wheat and similar proteins in barley and rye. The disease can cause different symptoms such as d...

Detailed Description

A symptom questionnaire will be administered at study initiation, 2 weeks and 12 weeks. Patients will undergo a breath test which involves drinking a sugar (lactulose) solution and breathing into a ma...

Eligibility Criteria

Inclusion

  • Adult patients age 18 or older
  • Biopsy proven celiac disease
  • Persistent symptoms of diarrhea, gas, bloating and/or cramping despite a gluten free diet for at least 1 month
  • Women that are not pregnant or lactating can be included. All women must have a documented negative pregnancy test at the initiation of the study. Women who become pregnant during the study will be asked to discontinue the study drug and will be followed up until the outcome of pregnancy is known. Women of child bearing potential must be practicing an effective method of birth control (eg: prescription oral contraceptive, contraceptive injections, intra-uterine device (IUD), double barrier method, contraceptive patch, male sterilization) before entry and throughout the treatment period.

Exclusion

  • antibiotic use for any indication within preceding one month
  • use of bismuth compounds within preceding month
  • concomitant use of pancreatic supplements
  • concomitant use of antispasmodics
  • concomitant use of immunomodulators such as corticosteroids, budesonide, alkylating agents and antimetabolites.
  • concomitant use of probiotics
  • concomitant use of prokinetic agents
  • concomitant use of 5-hydroxytryptamine receptor (5HT3) antagonists,5-hydroxytryptamine receptor (5HT4) antagonists.
  • concomitant use of antimotility agents (e.g loperamide)
  • concomitant use of antidiarrheal agents
  • diagnosed microscopic colitis or inflammatory bowel disease
  • other causes of malabsorption: pancreatic insufficiency, giardiasis and enteropathy associated with T cell lymphoma.
  • other diseases: renal or hepatic insufficiency.
  • pregnant patients and lactating females. In addition women of child bearing age will be excluded if they are not using one of the methods of contraception like oral contraceptives,intrauterine device.
  • and double barrier methods.
  • patients with tuberculosis or a positive purified protein derivative (PPD) test and infection with other mycobacterial diseases.
  • allergy and/or potential emergence of drug resistance to rifampicin and rifamycin compounds.

Key Trial Info

Start Date :

October 1 2006

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 1 2008

Estimated Enrollment :

50 Patients enrolled

Trial Details

Trial ID

NCT01137955

Start Date

October 1 2006

End Date

April 1 2008

Last Update

June 29 2022

Active Locations (1)

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1

Celiac Disease Center at Columbia University

New York, New York, United States, 10032