CompletedNot applicableNCT02175888
The Optimization of Bioavailability From Iron Supplements: Study 1
Studying Autosomal recessive sideroblastic anemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Swiss Federal Institute of Technology
- Principal Investigator
- Diego Moretti, PhDHuman Nutrition Laboratory, ETH Zurich
- Intervention
- Daily administration of 60 mg iron in form of ferrous sulphate capsules for 14 consecutive days(dietary_supplement)
- Enrollment
- 20 enrolled
- Eligibility
- 18-45 years · FEMALE
- Timeline
- 2015 – 2016
Study locations (1)
- Human Nutrition Laboratory, Zurich, Switzerland
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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