Status:
COMPLETED
Effect of Dexmedetomidine and Propofol on Regional Cerebral Tissue Oxygen Saturation
Lead Sponsor:
Ain Shams University
Conditions:
Regional Cerebral Tissue Oxygen Saturation
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
50 patients divided into 2 groups .Group I Dexmedetomidine infusion. Group II with Propofol infusion
Detailed Description
: 50 patients anticipated for open heart surgeries were encompassed in the study. Patients were divided into 2 groups, group P (receiving propofol) and group D (receiving dexmedetomidine) during CPB. ...
Eligibility Criteria
Inclusion
- Patients undergoing valve surgeries
- Patients undergoing on pump coronary artery bypass grafting surgeries
Exclusion
- emergency cases, patients with cervical spine pathology (cervical stenosis, cervical disc herniation, carotid stenosis), patients with cerebral pathology (cerebral strokes, ischemic attacks), patients with Mini Mental State Examination Score (MMSE) of 23 or less, complicated cases with prolongation of the cardiopulmonary bypass period, patients needing moderate hypothermia
Key Trial Info
Start Date :
June 15 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 21 2019
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT03817112
Start Date
June 15 2017
End Date
January 21 2019
Last Update
January 25 2019
Active Locations (1)
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1
Ain Shams Cardiothoracic hospital
Cairo, Egypt