Non-invasive Detection of Iron Deficiency in Obstetrics
Recruiting · NCT07083492 · Observational (researchers observe without assigning treatment) · Lead sponsor: Wuerzburg University Hospital
View the official record on ClinicalTrials.gov →Interventions studied
non-invasive measurement of zink protoporphyrin
What this trial is about
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.
Who can take part
Age range
18 Years and older
Sex
Female
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
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
Where it is running
1 location listed.
- University Hospital Würzburg - Würzburg, Bavaria, Germany