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The Effect of the Timing of Colloid and Crystalloid Infusions on Postspinal Hypotension After Spinal Anesthesia for Caesarian Section

NCT02680678 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2020-01-22

No results posted yet for this study

Summary

Prevention of postspinal hypotension after spinal anesthesia for caesarian section by use of preoperative or intraoperative volume replacement. The comparison of crystalloid and colloid infusions and their timing via perfusion index and plethysmographic variability index.

Conditions

  • Complications; Anesthesia, Spinal and Epidural, in Pregnancy

Interventions

OTHER

Colloid Preload

preload infusion

OTHER

colloid co-load

co-load infusion

OTHER

Crystalloid preload

preload infusion

OTHER

Crystalloid Co-load

co-load infusion

Sponsors & Collaborators

  • Balikesir University

    lead OTHER

Principal Investigators

  • Hafize Fisun Demir · Balikesir University School of Medicine Department of Anesthesia and Reanimation

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2014-04-30
Primary Completion
2016-08-31
Completion
2016-12-31

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT02680678 on ClinicalTrials.gov