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Clinical Trials/IRCT20160307026950N55
IRCT20160307026950N55
Recruiting
Phase 3

A comparative study of the sedative and analgesic effects of two combinations of dexmethomidine-ketamine (Ketodex) and propofol-fentanyl (Fenofel) in patients undergoing endoscopic retrograde cholangiopancreatography.

Esfahan University of Medical Sciences0 sites120 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Esfahan University of Medical Sciences
Enrollment
120
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

Eligibility Criteria

Inclusion Criteria

  • Age over 18 years
  • Consent to enter the study
  • Patients who are candidates for endoscopic retrograde cholangiopancreatography
  • Patients with American Society of Anesthesiologists (ASA) I,II

Exclusion Criteria

  • Patients with high blood pressure, coronary heart disease and central nervous system disorders
  • Patients with known allergies to study drugs
  • Airway's disease

Outcomes

Primary Outcomes

Not specified

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