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Clinical Trials/IRCT20231009059668N1
IRCT20231009059668N1
Recruiting
Phase 3

Comparing the Effect of Propofol-Dexmedetomidine versus Propofol in Anesthesia Induction in Patients with Major Depression or Bipolar-Disorder under Electroconvulsive therapy

Sanandaj University of Medical Sciences0 sites82 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Condition 1: Bipolar disorders. Condition 2: Major depression.
Sponsor
Sanandaj University of Medical Sciences
Enrollment
82
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Sanandaj University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Age 18 to 50 years
  • Patient in class 1 or 2 ASA physical status
  • Patient diagnosed with major depression or bipolar disorder referred by a psychiatrist

Exclusion Criteria

  • History of cardiovascular, kidney, liver and lung disease
  • History of other mental diseases, except major depression or bipolar disorder
  • History of head trauma
  • History of cardiovascular surgery
  • History of allergy to propofol or foods such as eggs or soybeans
  • Patient under treatment with bupropion and anticonvulsant
  • The attending physician's lack of consent for the patient's participation in the study

Outcomes

Primary Outcomes

Not specified

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