CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 84 enrolled
Drug / intervention
INVOS Cerebral Oximetrydevice
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/NCT02473978
NCT02473978N/ACompleted
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Cerebral Near-infrared Spectroscopy (NIRS) Monitoring Throughout Caesarean Deliveries

Rabin Medical Center·observational·Posted Jun 17, 2015·Updated May 10, 2016

In Brief

An observational study evaluating INVOS Cerebral Oximetry for Anoxia. Completed, enrolled 84 participants across 1 site.

Detailed Summary

In this study the investigator would like to examine hemodynamic cerebral blood flow and brain function by the use of Invos cerebral oximetry in women undergoing cesarean section delivery. This study is a purely observational study, it will not have any clinical intervention nor will it interfere with standard cesarean delivery protocols in any way. The investigator's primary objective is to evaluate how anesthesia influences cerebral blood flow perfusion during cesarean section deliveries.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsAnoxia
CountriesIsrael
Collaborators--

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedJun 17, 2015
Enrollment StartApr 1, 2015
Primary CompletionApr 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 11.0 years ago

Interventions

INVOS Cerebral Oximetrydevice

Participants will be connected to INVOS Cerebral Oximetry Cerebral Oximetry preoperativly and intraoperativly to ascess there cerebral perfusion throughout cesarean sections.