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Cerebral Near-infrared Spectroscopy (NIRS) Monitoring Throughout Caesarean Deliveries

NCT02473978 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 84

Last updated 2016-05-10

No results posted yet for this study

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.

Conditions

  • Anoxia

Interventions

DEVICE

INVOS Cerebral Oximetry

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

Sponsors & Collaborators

  • Rabin Medical Center

    lead OTHER

Principal Investigators

  • sharon orbach, md · Rabin Medical Center

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2016-04-30
Completion
2016-04-30

Countries

  • Israel

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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 NCT02473978 on ClinicalTrials.gov