Clinical Trials Directory

Trials / Completed

CompletedNCT03527680

Effect of Lactobacillus Rhamnosus on Serum Uremic Toxins in Hemodialysis

Effect of Lactobacillus Rhamnosus on Serum Uremic Toxins (Phenol and P-Cresol ) in Hemodialysis Patients: A Double Blind Randomized Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
42 (actual)
Sponsor
nooshin dalili · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

Uremic toxins such as p-cresol and phenol are suggested to be associated with higher mortality in hemodialysis patients. The aim of this study was to investigate the effects of probiotics on serum p-cresol level in hemodialysis patients.

Detailed description

Overall, 42 hemodialysis patients (10 women and 32 men) were divided randomly into the Lactobacillus rhamnosus group (21 patients) and the placebo group (21 patients).

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLactobacillus rhamnosusdaily one capsule containing 1.6\*107 CFU of Lactobacillus Rhamnosus prepared by Tabriz Nutrition Research Center from yogurt and cheese of different farms located in the suburbs Heris, after meal for 28 days
DRUGPlacebo - Capdaily one capsule of placebo

Timeline

Start date
2016-09-01
Primary completion
2016-11-30
Completion
2016-12-30
First posted
2018-05-17
Last updated
2018-05-17

Source: ClinicalTrials.gov record NCT03527680. Inclusion in this directory is not an endorsement.