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Clinical Trials/IRCT20200502047269N1
IRCT20200502047269N1RecruitingPhase 3

Comparison of the sedative effect of Remifentanil and Dexmidetomidine in patients undergoing venous arterial fistula implantation

Iran University of Medical Sciences0 sites32 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 3
Status
Recruiting
Enrollment
32

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
19 years to 60 years (—)
Sex
All

Inclusion Criteria

  • Age group 19 to 60 years
  • Patients with stable hemodynamic status

Exclusion Criteria

  • Patients with a history of cardiovascular abnormalities
  • Patients with a history of chronic diseases such as liver disease
  • Patients with a history of allergies to anesthetics, including opioids
  • Patients with a history of opium use
  • Pregnant or lactating women
  • Recent respiratory tract infection
  • Severe bronchopulmonary disease

Investigators

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