Clinical Trials Directory

Trials / Unknown

UnknownNCT03305705

Effect of Iron on Cerebral Dopamine Receptor Density in Non-anaemic Premenopausal Women With Low Ferritin and Fatigue

Double-Blind, Single-Center Interventional Trial To Evaluate The Effect Of Intravenous Iron Versus Placebo On Cerebral Dopamine Receptor Density In Non Anaemic Premenopausal Women With Low Ferritin Levels And Fatigue

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Albina Nowak, MD · Academic / Other
Sex
Female
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

Summary

This study investigates the effect of intravenous iron substitution in non-anaemic premenopausal women with iron deficiency on: * Changes in the cerebral Dopamine (DA) receptor density after iron substitution, shown by brain PET * Reduction of fatigue and other neuropsychological symptoms after iron supplementation

Conditions

Interventions

TypeNameDescription
DRUGIron CarboxymaltoseSingle intravenous infusion within 20 min
DRUGSodium chloride 0.9%Single intravenous infusion of 250 ml within 20 min

Timeline

Start date
2017-10-23
Primary completion
2019-08-31
Completion
2019-08-31
First posted
2017-10-10
Last updated
2017-10-13

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT03305705. Inclusion in this directory is not an endorsement.