Hydrogen Breath Test an Instrument to Predict Rifaximin-Response in Irritable Bowel Syndrome Predominant Diarrhea
Study Details
Study Description
Brief Summary
The purpose of this study is to learn more about how to improve treatment of patients with diarrhea predominant Irritable Bowel Syndrome (IBS-D) symptoms.Included patients will be requested to answer online surveys and will undergo treatment with rifaximin. Hydrogen breath testing and biologic samples collection will also be completed during the study.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Detailed Description
The study aims to determine whether hydrogen breath testing can be used to identify patients with IBS-D who are more likely to respond to rifaximin. Participating patients will complete a one week screening period when brief daily survey will be answered. Eligible patients will proceed with the treatment phase of the study, when patients will receive a 14 day course of rifaximin. All included patients will complete glucose and lactulose hydrogen breath tests before and after rifaximin treatment. Biological samples (e.g. blood, stool) will be collected at pre-determined time points and patients will answer daily brief survey for the duration of the study.
It is anticipated that 210 patients will be screened to reach a goal of enrolling 110 patients for the treatment phase of the study.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Rifaximin and breath tests Rifaximin 550mg three times a day for 14 days. Breath tests (glucose and lactulose) will be completed prior to Rifaximin treatment and at week 13 of the study. |
Drug: Rifaximin
Rifaximin will be given during weeks 2-4
Other Names:
Device: Glucose and lactulose hydrogen breath testing
Subjects will undergo glucose and lactulose hydrogen breath tests for Small Intestinal Bacterial Overgrowth (SIBO) on consecutive days using a commercially available home base kits (Glucose Hydrogen Breath Test Collection Kit and Lactulose Hydrogen Breath Test Collection Kit for SIBO from Commonwealth Diagnostic International) prior to Rifaximin treatment and at week 13 of the study.
|
Outcome Measures
Primary Outcome Measures
- Number of treatment responders [first 4 weeks after rifaximin treatment]
A responder is defined as a patient simultaneously meeting weekly response criteria for abdominal pain (≥30% decrease from baseline in mean weekly pain score) and stool consistency (≥50% decrease from baseline in number of days/week with Bristol Stool Scale type 6 or 7 stool) during ≥2 of the 4 weeks after treatment
Secondary Outcome Measures
- Severity of abdominal pain by numeric rating scale (0-10) [baseline (week 1), up to 12 weeks]
A responder is defined as a patient with ≥30% decrease from baseline in mean weekly worst pain.
- Stool consistency by Bristol Stool Form Scale (1-7) [baseline (week 1), up to 12 weeks]
A responder is defined as a patient with ≥ 50% decrease from baseline in number of days/weeks with Bristol stool scale type 6 or 7 stool.
- Severity of bloating by numeric rating scale (0-10) [baseline (week 1), up to 12 weeks]
A responder is defined as a patient with ≥ 30 % decrease from baseline in mean weekly worst bloating score.
- Severity of bowel urgency by rating scale (0-10) [baseline (week 1), up to 12 weeks]
A responder is defined as a patient with ≥ 30 % decrease from baseline in mean weekly worst urgency score.
- Compare the predictive value of a pre-treatment glucose vs. lactulose hydrogen breath test for symptomatic response to rifaximin in IBS-D patients. [baseline (week 1), up to 12 weeks]
Irritable Bowel Syndrome- Severity Scoring system (IBS-SSS) responder decrease in score of >75 points compared to baseline. The scoring range is from 0% to 500% with decreasing points indicating improvements in symptoms. Scores will be compared week 1 to those collected on weeks 4, 8, and 12.
- Irritable Bowel Syndrome - Quality of Life Measure responder [baseline (week 1), up to 12 weeks]
Defined as a decrease in score of 14 points from the baseline assessment. The score range is from 34 to 170, with decreasing in score indicating improvement in symptoms. Scores will be compared week 1 to those collected on weeks 4, 8, and 12.
- Compare the predictive value of a pre-treatment glucose or lactulose hydrogen breath test [first 4 weeks after rifaximin treatment]
We will compare the proportion of patients meeting the primary response definition stratified by positive or negative glucose or lactulose breath test results
Eligibility Criteria
Criteria
Inclusion Criteria:
-
IBS-D (Rome IV Diagnostic Criteria)
-
Diary compliance for at least 5 days and no rescue medications during baseline
-
Appropriate levels of abdominal pain and diarrhea
Exclusion Criteria:
-
Pregnant women or planning on becoming pregnant while in the study, or lactating women while in the study
-
Inflammatory bowel disease, diabetes mellitus, systemic sclerosis, or celiac disease
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Active gastrointestinal or hematological malignancy which requires ongoing treatment
-
Surgery to the GI tract in the past 3 months
-
Gastrointestinal infection or diverticulitis in the past 3 months
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Severe hepatic impairment
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Any use of antibiotics in the past month
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Current use of probiotics
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Any history of allergies to rifaximin or its derivatives
-
Any comitant use of P-glycoprotein inhibitors (for example. Cyclosporine)
-
Known allergies to glucose or lactulose
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Michigan | Ann Arbor | Michigan | United States | 48109 |
Sponsors and Collaborators
- University of Michigan
- Commonwealth Diagnostics International, Inc.
Investigators
- Principal Investigator: William Chey, M.D., University of Michigan
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- HUM00142925