CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 120 enrolled
Drug / intervention
phenylephrine infusion +2 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04404946
NCT04404946N/ACompleted

Colloid Co-hydration and Vasoconstrictor Infusion for Prevention of Postspinal Hypotension During Elective Cesarean Section. A Comparative Study

Aretaieion University Hospital·interventional·Posted May 28, 2020·Updated Jun 15, 2021

In Brief

A clinical study evaluating phenylephrine infusion, norepinephrine infusion, and 1 other intervention for Hypotension Symptomatic and 3 related conditions. Completed, enrolled 120 participants across 1 site.

Detailed Summary

This will be a double-blind randomized study, aiming at investigating a fixed rate phenylephrine infusion versus a fixed rate norepinephrine infusion versus placebo in combination with co-hydration with colloids for the prevention of maternal hypotension in elective cesarean section

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesGreece
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedMay 28, 2020
Enrollment StartMay 23, 2020
Primary CompletionMay 31, 2021
TodayJul 2, 2026
Enrollment to primary: 1.0 yearsPosted 6.1 years ago

Interventions

phenylephrine infusionother

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

norepinephrine infusionother

in parturients allocated to the norepinephrine group, a norepinephrine infusion will be started as soon as spinal anesthesia is initiated

placebo infusionother

in parturients allocated to the placebo group, a normal saline infusion will be started as soon as spinal anesthesia is initiated