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Prevention of Hypotension During Cesarean Section

NCT03842046 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 82

Last updated 2020-05-26

No results posted yet for this study

Summary

The aim of this double-blind randomized study will be to compare a fixed-rate prophylactic noradrenaline infusion to a fixed-rate prophylactic phenylephrine infusion during elective cesarean section under combined spinal-epidural anesthesia

Conditions

  • Hypotension Symptomatic
  • Obstetric Anesthesia Problems
  • Cesarean Section Complications
  • Vasoconstriction

Interventions

PROCEDURE

phenylephrine infusion

In parturients allocated to the phenylephrine group, a phenylephrine infusion will be initiated as soon as spinal anesthesia is established

PROCEDURE

norepinephrine infusion

In parturients allocated to the norepinephrine group group, a phenylephrine infusion will be initiated as soon as spinal anesthesia is established

Sponsors & Collaborators

  • Alexandra Hospital, Athens, Greece

    collaborator OTHER

  • Aretaieion University Hospital

    lead OTHER

Principal Investigators

  • Kassiani Theodoraki, PhD · Aretaieion University Hospital

  • Emmanouil Stamatakis, PhD · Alexandra General Hospital of Athens

  • Dimitrios Valsamidis, PhD · Alexandra General Hospital of Athens

  • Sofia Chatzilia, PhD · Alexandra General Hospital of Athens

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
48 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-16
Primary Completion
2019-08-31
Completion
2019-08-31

Countries

  • Greece

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 NCT03842046 on ClinicalTrials.gov