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Recruiting NCT07083492

Non-invasive Detection of Iron Deficiency in Obstetrics

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Trial Parameters

Condition Iron Deficiency Anemia of Pregnancy
Sponsor Wuerzburg University Hospital
Study Type OBSERVATIONAL
Phase N/A
Enrollment 500
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2022-11-15
Completion 2026-12-31
Interventions
non-invasive measurement of zink protoporphyrin

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Brief Summary

Validation of non-invasive measurement of zinc protoporphyrin for detection of iron deficiency in pregnancy. In addition, the impact of iron deficiency on the incidence of postpartum depression, restless legs syndrome, obstetric complications and quality of life will be examined.

Eligibility Criteria

Inclusion Criteria: * any timepoint during or up to 3 months after pregnancy * age ≥ 18 years * written informed consent Exclusion Criteria: * previous participation in this study * refusal of blood sampling * incapacity to give informed consent

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VIEW ON CLINICALTRIALS.GOV ↗ MORE IRON DEFICIENCY ANEMIA OF PREGNANCY TRIALS
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