Impact of Rifaximin Therapy on Intestinal Byproducts in End-Stage Renal Disease



Status:Withdrawn
Conditions:Renal Impairment / Chronic Kidney Disease, Renal Impairment / Chronic Kidney Disease
Therapuetic Areas:Nephrology / Urology
Healthy:No
Age Range:18 - Any
Updated:3/2/2019
Start Date:January 2016
End Date:February 26, 2019

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The purpose of this study is to determine if rifaximin reduces serum trimethylamine-N-oxide
(TMAO) levels in patients with end-stage renal disease.

Study participants will undergo 3 study visits: baseline, day 7 (immediately post-therapy),
day 21 (2 weeks post-therapy). All participants will provide blood and stool samples at each
visit.

Inclusion Criteria:

- Diagnosis of end-stage renal disease

- Receiving chronic intermittent hemodialysis

Exclusion Criteria:

- Patients with less advanced kidney disease

- Inability or unwillingness to provide informed consent

- Patients who may be pregnant

- Hemodynamically unstable patients

- Patients with liver failure, pancreatic insufficiency, or inflammatory bowel disease

- Patients with ongoing or recent infection and those with history of C-diff infection

- Patients with abnormal bowel structure secondary to surgical or anatomic variations

- Patients on certain medications, including immunosuppressants, antidiarrheal agents,
or recent (within the last 2 months) use of antibiotics
We found this trial at
2
sites
Westwood, Kansas 66205
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3901 Rainbow Blvd
Kansas City, Kansas 66160
(913) 588-5000
University of Kansas Medical Center The University of Kansas Medical Center serves Kansas through excellence...
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