CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 82 enrolled
Drug / intervention
phenylephrine infusion +2 moredrug
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/NCT00846651
NCT00846651Phase 4Completed

Comparison of Phenylephrine Infusion With Colloids vs. Crystalloids for Reduction of Spinal-induced Hypotension During Cesarean Section

Milton S. Hershey Medical Center·interventional·Posted Feb 19, 2009·Updated Oct 16, 2017

In Brief

A Phase 4 clinical trial evaluating Colloid administration, Crystalloid administration, and 1 other intervention for Hypotension. Completed, enrolled 82 participants across 1 site.

Detailed Summary

The purpose of this study is to compare two methods for preventing low blood pressure associated with spinal anesthesia during Cesarean sections.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHypotension
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedFeb 19, 2009
Enrollment StartFeb 1, 2009
Primary CompletionDec 1, 2009
Study CompletionFeb 1, 2010
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 17.4 years ago

Interventions

Colloid administrationother

The patients received 0.5 L colloid solution (hydroxyethylstarch 6%) or 1.5 L Ringer lactate prior to spinal anesthesia for cesarean section.

Crystalloid administrationother

The patients received 1.5 L Ringer lactate prior to spinal anesthesia for cesarean section.

phenylephrine infusiondrug

A phenylephrine infusion will be started immediately after performing the spinal anesthesia and continued until time of uterine incision.