Pregnancy Trimester, First, Pregnancy Trimester, Second, Pregnancy Trimester, Third
Conditions
Keywords
G08.520.769.550.408, G08.520.769.550.490, G08.520.769.550.520
Brief summary
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.
Detailed 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.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Pregnant women without major concomitant disease * Willing and able to provide informed consent * Age (three age groups): * 20 to 22 years * 30 to 32 years * 40 to 42 years
Exclusion criteria
* Non pregnant women * Men * No informed consent * Age not included in inclusion criteria * Major concomitant disease
Countries
Germany