MedTrace Logo

Colloid Preload Versus Crystalloid Co-load in Cesarean Section Under Spinal Anesthesia

NCT03107598 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 127

Last updated 2017-04-11

No results posted yet for this study

Summary

Comparison between colloid preload and crystalloid co-load in cesarean section under spinal anesthesia.

1. The primary outcome was the incidence of hypotension
2. Secondary outcomes included the incidence of severe hypotension, total ephedrine dose, nausea and vomiting and neonatal outcome assessed by Apgar scores and umbilical artery blood gas analysis

Conditions

Interventions

DRUG

colloid preload

coparaison between colloid and crystalloide loading in spinal anesthesia for cesarean section

Sponsors & Collaborators

  • University Hospital, Mahdia

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-03-31
Primary Completion
2016-09-30
Completion
2016-09-30

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 NCT03107598 on ClinicalTrials.gov