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Sucrosom5al Iron Supplementation in Blood Donors

NCT04250298 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2025-09-16

Study results available
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Summary

The aim of this descriptive/explorative pilot study is to examine the effects of supplementing a sucrosomial iron preparation in whole blood donors with iron deficiency for three months.

Conditions

  • Iron-deficiency

Interventions

DIETARY_SUPPLEMENT

sucrosomial iron

oral intake of iron as sachets or capsules

Sponsors & Collaborators

  • Johannes Kepler University of Linz

    collaborator OTHER

  • Fresenius Kabi

    collaborator INDUSTRY

  • Medical University of Graz

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-11-13
Primary Completion
2020-09-28
Completion
2020-12-20

Countries

  • Austria

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04250298 on ClinicalTrials.gov