Ferrous Sulphate Supplement in Women With Iron Deficiency Anaemia

Status Completed

Clinical Trial Summary

The purpose of this study is to investigate the pharmacokinetics of serum iron (the amount of iron in blood) after single oral administration of 2 tablets of L0008 80 mg (as ferrous sulphate) in women with iron deficiency anaemia.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01757119
Study type	Interventional
Source	Pierre Fabre Medicament
Contact
Status	Completed
Phase	Phase 1
Start date	January 2013
Completion date	March 2014

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See also
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