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
| Type | Name | Description |
|---|---|---|
| DRUG | L-carnitine | 500 mg,twice daily, 16 weeks |
| DRUG | placebo | 500 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.