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Evaluation of Copeptin Levels in Elective Cesarean Section With Different Anesthetic Technique

NCT03536910 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2019-02-26

No results posted yet for this study

Summary

In this study, investigators aimed to investigate the effects of general and spinal anesthesia techniques on copeptin levels during cesarean section and their relation with fetal distress.

Conditions

  • Fetal Distress

Interventions

OTHER

Copeptin

Level of copeptin in maternal blood and umbilical cord blood

Sponsors & Collaborators

  • Istanbul University

    lead OTHER

Principal Investigators

  • Ece YAMAK ALTINPULLUK, MD · Istanbul University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2018-05-01
Primary Completion
2018-07-31
Completion
2018-10-31

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 NCT03536910 on ClinicalTrials.gov