cardiac burden childbirth
Conditions
Interventions
None listed
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: - Informed consent - Being in active labour (defined as progressing cervical dilatation) o Or currently being induced for labour o Or planned primary Caesarean section
Exclusion criteria
Exclusion criteria: - Age
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary study outcome is the difference in CO trajectory during labour between the cardiac and non-cardiac group. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary study outcomes are differences in the impact of obstetric interventions (e.g. epidural analgesia or assisted delivery) on CO trajectory. In addition to CO trajectory, additional hemodynamic parameters (e.g. heart rate and blood pressure) will be measured. | — |
Countries
Netherlands
Outcome results
None listed