Trials / Completed
CompletedNCT01380548
Effects of 5-Aminolevulinic Acid on Iron Deficiency Anemia
A Double-blind, Placebo Controlled Study to Assess Efficacy of 5-Aminolevulinic Acid in Subjects With Iron Deficiency Anemia
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 135 (estimated)
- Sponsor
- Hiroshima University · Academic / Other
- Sex
- Female
- Age
- 20 Years – 49 Years
- Healthy volunteers
- Not accepted
Summary
This study is designed to evaluate efficacy and dose-dependency of 5-aminolevulinic acid in subjects with iron deficiency anemia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Placebo | Placebo; once/day; for 12 weeks |
| DIETARY_SUPPLEMENT | Iron alone | Iron (3 mg); once/day; for 12 weeks |
| DIETARY_SUPPLEMENT | Low-dose 5-aminolevulinic acid with iron | 5-Aminolevulinic acid (12.5 mg) and iron (3 mg); once/day; for 12 weeks |
| DIETARY_SUPPLEMENT | Medium-dose 5-aminolevulinic acid with iron | 5-Aminolevulinic acid (25 mg) and iron (3 mg); once/day; for 12 weeks |
| DIETARY_SUPPLEMENT | High-dose 5-aminolevulinic acid with iron | 5-Aminolevulinic acid (50 mg) and iron (3 mg); once/day; for 12 weeks |
Timeline
- Start date
- 2011-06-01
- Primary completion
- 2012-12-01
- Completion
- 2012-12-01
- First posted
- 2011-06-27
- Last updated
- 2013-03-28
Locations
1 site across 1 country: Japan
Source: ClinicalTrials.gov record NCT01380548. Inclusion in this directory is not an endorsement.