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Safety and Effectiveness of IHAT in Iron Deficient Pre-menopausal Woman

Iron-deficiency Clinical Trial

Official title:
A Randomised, Double-blind Study to Determine the Safety and Efficacy of IHAT in Iron Deficient Premenopausal Women.

Clinical Trial Summary

This is a double blind, randomised, placebo-controlled trial to evaluate orally-dosed IHAT (iron hydroxide adipate tartrate) at 2 different doses compared to placebo for increasing serum ferritin levels in iron-deficient but otherwise healthy premenopausal women over 12 weeks.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05950841
Study type Interventional
Source RDC Clinical Pty Ltd
Contact Amanda Rao, PhD
Phone +61 414 488 559
Email amanda@rdcglobal.com.au
Status Not yet recruiting
Phase Phase 3
Start date January 1, 2024
Completion date December 1, 2025
View Details
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