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Clinical Trials/TCTR20200324003
TCTR20200324003
Enrolling By Invitation
Phase 2

Comparison postoperative delirium within 24 hours between ketamine and propofol as a main anesthetic agent during cardiopulmonary bypass machine

none0 sites82 target enrollmentMarch 24, 2020
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Conditionsperioperative strokedeathre&#45operationpostoperative deliriumcardiac surgeryketaminecognitive dysfunction

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
perioperative strokedeathre&#45
Sponsor
none
Enrollment
82
Status
Enrolling By Invitation
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 24, 2020
End Date
March 16, 2020
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
none

Eligibility Criteria

Inclusion Criteria

  • •patients who are elderly (≥65 years old) of both genders.
  • •patients who have less than 4 euroscore.
  • •patient without language barrier.
  • •patients who undergo cardiac operation performed under general anesthesia with cardiopulmonary bypass.

Exclusion Criteria

  • •patients who known preoperative cognitive disorder (dementia, cognitive impairment)
  • •patients who've got positive CAM and RASS
  • •patients who have psychiatric or mental disorder
  • •patients who have cerebrovascular disease or carotid disease
  • •patients who undergo aortic surgery
  • •patients who died intra\-operatively or within the first 24 hours after the procedure and re\-operative patients.

Outcomes

Primary Outcomes

Not specified

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