Overview

ED50 Determination of Hydroxyethylstarch for Treatment of Hypotension During Cesarean Section Under Spinal Anesthesia

Status:
Unknown status

Trial end date:
2013-06-01

Target enrollment:

Participant gender:

Summary

The purpose of this trial is to determine the effective volume of hydroxyethylstarch 130/0.4 which would prevent the occurence of maternal hypotension in 50% of healthy pregnant women undergoing a cesarean section under spinal anesthesia.

Phase:

Phase 4

Details

Lead Sponsor:

Maisonneuve-Rosemont Hospital

Collaborator:

Université de Montréal

Treatments:

Anesthetics
Hydroxyethyl Starch Derivatives