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The Study of Omega-3 supplementation Effect on Lipid Profiles in Hemodialysis Patients

Not Applicable
Conditions
hemodialysis patients.
End-stage renal disease
Registration Number
IRCT2013081214333N1
Lead Sponsor
Vice Chancellor for Research Affairs, Kermanshah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Inclusion criterias: patient's willingness to cooperate, and at least 6 months of dialysis starting time. Exclusion criterias: presence of bleeding and warfarin anticoagulation drugs usage or anti-thrombotic (aspirin, ticlopidine, dipyridamole and clopidogrel); diabetes; hepatitis, and other infectious diseases; body mass index less than 18.5 or more than 30 kg/ m2; steroidal and non-steroidal anti-inflammatory drugs; omega-3 fatty acids supplements and vitamins E or C within two months before the study .

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cholestrol. Timepoint: week,0,10. Method of measurement: by cell counter.;Triglycerid. Timepoint: week,0,10. Method of measurement: by sell counter.;H.d.L. Timepoint: week,0,10. Method of measurement: by cell counter.;L.D.L. Timepoint: week,0,10. Method of measurement: by cell counter.;Serum alboumin. Timepoint: weak ,0,10. Method of measurement: by sell counter.
Secondary Outcome Measures
NameTimeMethod
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