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Status: | Withdrawn |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