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Symbiotic and blood uremic toxins in hemodialysis patients

Phase 2
Conditions
end stage renal disease.
Hypotension of hemodialysis
Registration Number
IRCT20160528028120N1
Lead Sponsor
Isfahan university of medical sciences; research assistant part
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
46
Inclusion Criteria

performing hemodialysis treatment 3-times per week for at least 4 hours each time,
not being pregnant or lactating
no history of active cancers (except for skin cancer)
no history of severe chronic conditions such as pulmonary, cardiovascular, and hepatic diseases
lack of gastrointestinal disorders, HIV disease, and psychiatric problems

Exclusion Criteria

those who used symbiotic, probiotic, prebiotic or antibiotics during 4 weeks preceding the study
those who used immune suppressive medicines, and anticoagulant agents
with severe edema
addiction to alcohol or drugs abuse
did not respond to the questions honestly
and reported any side effects due to synbiotic consumption

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Indoxyl sulfate. Timepoint: 1 and 8 weeks of treatment. Method of measurement: Eliza kit.;Crp. Timepoint: 1 and 8 weeks of treatment. Method of measurement: Eliza kit.
Secondary Outcome Measures
NameTimeMethod
Phenol. Timepoint: 1 and 8 weeks of treatment. Method of measurement: hplc.
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