Phenylephrine for Spinal Induced Hypotension

Status Completed

Clinical Trial Summary

This study is designed to determine the ED90 for a single dose of phenylephrine for the treatment of spinal induced hypotension in parturients presenting for an elective CD. The ED90 is the effective dose at which 90% of subjects will have a "positive" response to phenylephrine. The primary outcome measure is the ED90 for bolus phenylephrine. Secondary outcomes include the need for additional vasopressors, glycopyrolate to treat bradycardia, and the presence of hypertension following administration of phenylephrine.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Hypotension

Clinical Trial Details

NCT number	NCT00781157
Study type	Interventional
Source	IWK Health Centre
Contact
Status	Completed
Phase	Phase 4
Start date	January 2008
Completion date	October 2008

View Details

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