Ireland
--:--IST
Recruiting Observational

Non-invasive Detection of Iron Deficiency in Obstetrics

NCT07083492 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2022-11-15
Last updated
2025-07-24

Condition(s) studied

Iron Deficiency Anemia of PregnancyIron-deficiencyRestless Leg Syndrome in PregnancyRestless Leg Syndrome Due to Iron Deficiency AnaemiaPostpartum HemorrhagePostpartum DepressionPregnancy AnemiaIron Deficiency (Without Anemia)

Investigational drug(s) / intervention(s)

non-invasive measurement of zink protoporphyrin

non-invasive measurement of zink protoporphyrin: validation of non-invasive measurement of zink protoporphyrin

Study 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

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
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

Primary outcome measure(s)

  • Accuracy of non-invasive zinc protoporphyrin for the detection of iron deficiency in pregnancy — through study completion, up to 3 months postpartum
    To validate accuracy of non-invasively measured ZnPP for detection of iron deficiency in pregnancy at prespecified timepoints

Trial sites (1)

FacilityCityRegionStatus
University Hospital Würzburg Würzburg Bavaria Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07083492 on ClinicalTrials.gov ↗ ← All trials in Germany