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About
This is a single-centre, open, parallel-group study with three age groups; no study medication or intervention will be provided. This is a longitudinal follow-up of physiological parameters.
Full description
The subjects will be investigated as outpatients. For each subject, 4 individual dates with a duration of approximately 30 minutes each are scheduled - at the end of the first trimenon, at the end of the second trimenon, 4 weeks prior to the calculated date of birth, and 6 weeks after the effective date of birth.
Sex
Ages
Volunteers
Inclusion criteria
Pregnant women without major concomitant disease
Willing and able to provide informed consent
Age (three age groups):
Exclusion criteria
0 participants in 3 patient groups
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Data sourced from clinicaltrials.gov
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