drugset / Trial / NCT04309669

Assessment of the eFficacy, the Onset-of-Action and the Safety of Tot'héma® in Adults With Moderate Iron Deficiency Anaemia

NCT04309669

Phase 4 Completed 167 enrolled Laboratoire Innotech International
NaSingle-groupOpen-labelTreatment

Summary

The aim of this study is to assess, in patients with moderate IDA, the Onset-of-Action of a daily treatment with Tot'Héma®. The onset of action is defined as the time required for a mean increase of at least 0,5g/dL from baseline in the haemoglobin level.

Timeline

Start
2020-11-12
Primary completion
2023-10-06
Completion
2023-10-06

Drugs

EvaluationDrugModalityDoseRoute
Subject FERROUS GLUCONATE ANHYDROUS Small molecule 150 mg Oral
Background Copper Unknown Oral
Background manganese gluconate Unknown Oral

Indications