N/A
N=50
Rifaximin for the Treatment of Persistent Symptoms in Patients With Celiac Disease
Celiac Disease
Bottom Line
View on ClinicalTrials.gov: NCT01137955 ↗Enrolled (actual)
50
Serious AEs
0.0%
Results posted
Jun 2022
Primary outcome: Primary: Baseline Gastrointestinal Symptom Rating Scale (GSRS) Score — 2.7; 2.8 Score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Rifaximin (Drug); Placebo (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Columbia University
- Primary completion
- Apr 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Baseline Gastrointestinal Symptom Rating Scale (GSRS) Score |
2.7; 2.8 | — |
| PRIMARY Week 2 Gastrointestinal Symptom Rating Scale (GSRS) Score |
2.3; 2.4 | — |
| PRIMARY Week 12 Gastrointestinal Symptom Rating Scale (GSRS) Score |
2.5; 2.5 | — |
| SECONDARY Percentage of Participants With Abnormal Breath Test |
12; 20 | — |
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 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.
Eligibility Criteria
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.
Data sourced from ClinicalTrials.gov (NCT01137955). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.