Clinical Trials Directory

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

TypeNameDescription
DIETARY_SUPPLEMENTPlaceboPlacebo; once/day; for 12 weeks
DIETARY_SUPPLEMENTIron aloneIron (3 mg); once/day; for 12 weeks
DIETARY_SUPPLEMENTLow-dose 5-aminolevulinic acid with iron5-Aminolevulinic acid (12.5 mg) and iron (3 mg); once/day; for 12 weeks
DIETARY_SUPPLEMENTMedium-dose 5-aminolevulinic acid with iron5-Aminolevulinic acid (25 mg) and iron (3 mg); once/day; for 12 weeks
DIETARY_SUPPLEMENTHigh-dose 5-aminolevulinic acid with iron5-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.