Clinical Trials Directory

Trials / Completed

CompletedNCT01278693

Effect of Oral L-carnitine Supplement on Lipid Profile, Anemia, and Quality of Life of Patients

Study of Treatment of Dyslipidemia for Hemodialysis

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
54 (actual)
Sponsor
Isfahan University of Medical Sciences · Academic / Other
Sex
Female
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine Effect of oral L-carnitine supplement on lipid profile, anemia, and quality of life.

Detailed description

In patients under maintenance hemodialysis several factors reduce the body stored carnitine which in turn affected dyslipidemia, anemia, and general health in these patients. The investigators evaluated the effect of oral L-carnitine supplementation on lipid profiles, anemia, and quality of life in hemodialysis patients.

Conditions

Interventions

TypeNameDescription
DRUGL-carnitine500 mg,twice daily, 16 weeks
DRUGplacebo500 mg,twice daily, 16 weeks.

Timeline

Start date
2009-08-01
Primary completion
2010-09-01
Completion
2010-09-01
First posted
2011-01-19
Last updated
2011-01-19

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT01278693. Inclusion in this directory is not an endorsement.