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Norepinephrine and Phenylephrine for Maternal Cardiac Output During Spinal Anesthesia for Elective Cesarean Delivery

NCT02969239 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2017-03-10

No results posted yet for this study

Summary

The purpose of this study is to compare norepinephrine and phenylephrine on the effects of maintaining the cardiac output in Cesarean section under spinal anesthesia.

Conditions

Interventions

DRUG

Norepinephrine

bolus administered norepinephrine 5mcg intravenously, if SBP \<90mmHg or 20% decrease from baseline

DRUG

Phenylephrine

bolus administered phenylephrine 100mcg intravenously, if SBP \<90mmHg or 20% decrease from baseline

Sponsors & Collaborators

  • Jeju National University Hospital

    lead OTHER

Principal Investigators

  • AE RYOUNG LEE · Jeju National University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2017-07-31
Completion
2017-07-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02969239 on ClinicalTrials.gov