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Colloid Preload Versus Colloid Coload During Cesarean Deliveries

NCT02393196 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2015-11-17

No results posted yet for this study

Summary

The investigators aimed to compare the methods colloid preloading and colloid coloading in terms of the incidence of maternal hypotension and impacts on neonatal outcomes. The second aim while planning the present study is to identify the method of the lowest adverse event for mother and infant and the simplest approach for the clinician.

Conditions

  • Anesthesia; Adverse Effect, Spinal and Epidural
  • Hypotension

Interventions

DRUG

hydroxyethyl starch (% 6 HES 130/0.4) (Voluven®)

Before spinal anesthesia

DRUG

hydroxyethyl starch (%6 HES 130/0.4) (Voluven®)

Just after spinal anesthesia

Sponsors & Collaborators

  • Sifa University

    lead OTHER

Principal Investigators

  • Aysun Afife Kar, MD · Şifa Üniversitesi, Basmane Hastanesi, İzmir, Turkey

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2016-01-31
Completion
2016-03-31

Countries

  • Turkey (Türkiye)

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 NCT02393196 on ClinicalTrials.gov