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Clinical Trial Summary

50 patients divided into 2 groups

.Group I Dexmedetomidine infusion. Group II with Propofol infusion


Clinical Trial 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. Both groups were studied for variations in right and left rScO2 as well as postoperative cognitive dysfunction using the Mini Mental State Examination Score (MMSE) test. ;


Study Design


Related Conditions & MeSH terms

  • Regional Cerebral Tissue Oxygen Saturation

NCT number NCT03817112
Study type Interventional
Source Ain Shams University
Contact
Status Completed
Phase N/A
Start date June 15, 2017
Completion date January 21, 2019