ClinicalTrials.Veeva

Menu

Hemodynamic Measurements During Cesarean Section With Spinal Anesthesia

University of Oslo (UIO) logo

University of Oslo (UIO)

Status and phase

Completed
Phase 4

Conditions

Healthy

Treatments

Drug: Phenylephrine

Study type

Interventional

Funder types

Other

Identifiers

NCT00199784
EudraCT2004-004902-26/S-05049
Elangesectio2005-1

Details and patient eligibility

About

The purpose of this study is to determine the effect of low dose versus standard dose spinal anesthesia with and without intravenous phenylephrine-infusion on blood pressure, cardiac output and systemic vascular resistance.

Full description

Hypotension during cesarean section with spinal anesthesia is common. We compare low dose versus standard dose spinal anesthesia with and without intravenous phenylephrine-infusion.

Enrollment

80 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Healthy pregnant women for elective cesarean section

Exclusion Criteria

  • Shorter than 160 or taller than 180 cm
  • Pre-pregnant body mass index (BMI) over 32

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems