Clinical Trial: Safety and Effectiveness of IHAT in Iron Deficient Pre-menopausal Woman
Study Status: COMPLETED
Recruit Status: COMPLETED
Condition: Iron-deficiency
Study Type: INTERVENTIONAL
Official Title: A Randomised, Double-blind Study to Determine the Safety and Efficacy of IHAT in Iron Deficient Premenopausal Women.
Brief 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.
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