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Completed

NCT Number: NCT01137955

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

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 diarrhea, bloating, abdominal pain and weight loss. The majority of patients respond to a gluten-free diet. However some patients (5-30%) have persistent symptoms and are considered to be poor responders to the diet. Bacterial overgrowth in the small intestine accounts for some of the refractory patients.

This study seeks to determine if antibiotic therapy with rifaximin relieves the symptoms of patients who are poorly responsive to a gluten-free diet and whether this impacts their breath test results.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Celiac Disease Center at Columbia University

New York, 10032, United States

About this study

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 machine. This technique will identify the presence of bacteria in the small intestine. They will be randomly selected to receive either an antibiotic (rifaximin) or placebo three times a day for 10 days to treat their bacterial overgrowth.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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 criteria

  • 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.

Treatment and study plan

Rifaximin

Drug

Rifaximin 400mg orally three times a day for 10 days total

Other names: Placebo orally three times a day for 10 days total

Placebo

Drug

Placebo orally three times a day for 10 days total

Other names: Rifaximin 400 mg orally three times a day for 10 days total

Primary outcomes

  1. Baseline Gastrointestinal Symptom Rating Scale (GSRS) Score

    Time frame: Baseline (week 0)

    Validated seven point questionnaire that assesses gastrointestinal symptoms for five symptom areas, including abdominal pain, reflux, indigestion, diarrhea, and constipation. Individual scores are calculated for each symptom area and the mean of the scores is used to derive an overall GSRS score. Scores range from 0-7, with higher scores indicating gastrointestinal discomfort.

  2. Week 2 Gastrointestinal Symptom Rating Scale (GSRS) Score

    Time frame: Week 2

    Validated seven point questionnaire that assesses gastrointestinal symptoms for five symptom areas, including abdominal pain, reflux, indigestion, diarrhea, and constipation. Individual scores are calculated for each symptom area and the mean of the scores is used to derive an overall GSRS score. Scores range from 0-7, with higher scores indicating gastrointestinal discomfort.

  3. Week 12 Gastrointestinal Symptom Rating Scale (GSRS) Score

    Time frame: Week 12

    Validated seven point questionnaire that assesses gastrointestinal symptoms for five symptom areas, including abdominal pain, reflux, indigestion, diarrhea, and constipation. Individual scores are calculated for each symptom area and the mean of the scores is used to derive an overall GSRS score. Scores range from 0-7, with higher scores indicating gastrointestinal discomfort.

Secondary outcomes

  1. Percentage of Participants With Abnormal Breath Test

    Time frame: Up to 12 weeks

    A breath test measures for small intestine bacterial overgrowth (SIBO). The breath test measures the amount of hydrogen exhaled after drinking a sugar (lactulose) solution. An abnormal breath test is defined as: 1) a rise in hydrogen of ≥20 parts per million (ppm) within 100 minutes, or 2) two peaks ≥20 ppm over baseline.

Sponsors and collaborators

Lead sponsor

Columbia University

Other

Collaborators

  • Bausch Health Americas, Inc.

Registry information

Official study title

Double-blind Randomized Controlled Trial of Rifaximin for Persistent Symptoms in Patients With Celiac Disease

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Jun 7, 2010
Registry last updated
Jun 29, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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