Non-invasive Detection of Iron Deficiency in Obstetrics
Recruiting
Observational Study
Iron Deficiency Anemia of Pregnancy
Iron-deficiency
Restless Leg Syndrome in Pregnancy
Restless Leg Syndrome Due to Iron Deficiency Anaemia
Postpartum Hemorrhage
Postpartum Depression
Pregnancy Anemia
Iron Deficiency (Without Anemia)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Observational
- Participants needed
- 500 (estimated)
- Sponsor
- Wuerzburg University Hospital · Other
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About This Trial
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.
Trial Locations
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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
Contacts