Non-invasive Detection of Iron Deficiency in Obstetrics
Condition(s) studied
Investigational drug(s) / intervention(s)
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| University Hospital Würzburg | Würzburg | Bavaria | Recruiting |
More Wuerzburg University Hospital trials in Germany
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