Anoxia Clinical Trial
Official title:
Cerebral Near-infrared Spectroscopy (NIRS) Monitoring Throughout Caesarean Deliveries
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.
This is a prospective, single center study which will be conducted at the Rabin Medical
Center (Beilinson Campus), Petach Tikva, Israel, a tertiary university hospital. The
Institutional Review Board has approved this study.
Two hundred women undergoing cesarean sections will be enrolled after filling out an
informed consent form.
Cerebral blood flow perfusion will be monitored preoperatively, intraoperativly and half an
hour postoperativly, for all enrolled participants using INVOS Cerebral Oximetry.
Preoperative data will be compared to intraoperative data and analyzed in order to evaluate
the dynamic cerebral oxygen and blood perfusion changes in women undergoing cesarean
sections.
;
Observational Model: Case-Crossover, Time Perspective: Cross-Sectional
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