Fluid Coloading and the Incidence of Hypotension

NCT01741610 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2014-01-15

No results posted yet for this study

Summary

This study was conducted to evaluate the effects of rapid crystalloid (Lactated Ringer's solution) or colloid (hydroxyethyl starch; HES) cohydration with a second intravenous access line on the incidence of hypotension and ephedrine requirement during spinal anaesthesia for caesarean section.

Conditions

  • Complications; Cesarean Section
  • Anesthesia; Adverse Effect, Spinal and Epidural
  • Other Fluid Overload

Interventions

BIOLOGICAL

Cristalloid and colloid coloading

Cristalloid coloading (Group L) Colloid coloading (Group C) No coloading (Group E)Placebo Comparator

Sponsors & Collaborators

  • Cukurova University

    lead OTHER

Principal Investigators

  • Hakki Unlugenc, Prof Dr · Cukurova University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
19 Years
Max Age
46 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-10-31
Primary Completion
2011-08-31
Completion
2012-06-30

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

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 NCT01741610 on ClinicalTrials.gov