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Clinical Trials/NCT01669135
NCT01669135
Completed
Not Applicable

Spinal Anesthesia for Cesarean Delivery is Associated With Decreases in Regional Cerebral Oxygen Saturation as Assessed by Near- Infrared Spectroscopy

University of Athens1 site in 1 country34 target enrollmentDecember 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cerebral Oxygen Saturation During Spinal Anesthesia for Cesarean Delivery
Sponsor
University of Athens
Enrollment
34
Locations
1
Primary Endpoint
cerebral oxygen saturation of the right frontal lobe
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The cerebral oxygen saturation is assessed by means of near-infrared spectometry in parturients undergoing cesarean delivery under spinal anesthesia. The investigators hypothesis was that spinal anesthesia does not influence cerebral oxygen saturation.

Registry
clinicaltrials.gov
Start Date
December 2010
End Date
August 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
University of Athens
Responsible Party
Principal Investigator
Principal Investigator

Argyro Fassoulaki

MD, PhD, DEAA

University of Athens

Eligibility Criteria

Inclusion Criteria

  • Term healthy parturients

Exclusion Criteria

  • Body Mass Index \> 35
  • preeclampsia
  • neurological,cardiovascular, respiratory disease

Outcomes

Primary Outcomes

cerebral oxygen saturation of the right frontal lobe

Time Frame: Change from the performing of spinal anesthesia untill 1 minute after delivery

Cerebral oxygen saturation is important as it may affect patient's outcome

Secondary Outcomes

  • cerebral oxygen saturation of the left frontal lobe(5, 10, 50 min after spinal,1 minute after delivery)
  • Thigh oxygen saturation(5, 10, 50 min after spinal, 1 minute after delivery)
  • Arterial Oxygenation(5, 10, 50 min after spinal, 1 minute after delivery)

Study Sites (1)

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