I97
Conditions
Interventions
Group 1: Patients treated with intermittent bolus doses of norepinephrine who also received 4 mg of ondansetron preoperatively.
Blood pressure readings are recorded at standardized time points during
Sponsors
Klinikum Bremen Mitte, Klinik für Anästhesiologie und Schmerztherapie
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Pregnancy, Delivery via cesarean section
Exclusion criteria
Exclusion criteria: No consent of mother after providing information of scope and nature of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary Endpoint: Maternal blood pressure levels The Blood Pressure values are routinely measured and documented during the course of the operation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Newborn outcome: APGAR, umbilical pH and Base excess The values are routinely measured and documented after the birth of the child. | — |
Countries
Germany
Contacts
Public ContactMichael Winterhalter
Klinikum Bremen Mitte
Outcome results
None listed