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Clinical Trials/IRCT20190212042688N1
IRCT20190212042688N1
Recruiting
Phase 3

A Comparison of Dexmedetomidine and Propofol in sedation efficacy in patients with elective upper gastrointestinal endoscopy

Zahedan University of Medical Sciences0 sites60 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
pper gastrointestinal disorders.
Sponsor
Zahedan University of Medical Sciences
Enrollment
60
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Zahedan University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • patients with elective upper gastrointestinal endoscopy
  • ASA class \=3

Exclusion Criteria

  • Having cardiovascular disease (arrhythmia, AS, IHD, HTN, HF or EF \<30%)
  • Having liver disease (Child\-Pugh Classification C)
  • Having kidney disease (GFR \<60%)
  • Having psychiatric illness (Major Depression, Mania, Psychosis)
  • Having Drug Addiction
  • Egg and soy allergy
  • Emergency endoscopy

Outcomes

Primary Outcomes

Not specified

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