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Clinical Trials/IRCT20230701058625N1
IRCT20230701058625N1
Recruiting
Phase 4

Comparison of the effectiveness of two treatment protocols dexmedetomidine - propofol and midazolam - fentanyl - propofol in relieving pain in patients undergoing lithotomy

Dezfoul University of Medical Sciences0 sites40 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Dezfoul University of Medical Sciences
Enrollment
40
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
Dezfoul University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Patients with kidney stones below 2cm and proximal ureter for ESWL aged 18 to 80 years with American Society of Anesthesiologists (ASA) physical status I, II or III who consent to participate in this study will be eligible for this study.

Exclusion Criteria

  • Patients who do not agree to participate in this study
  • Patients with chronic liver failure
  • Patients who have a history of allergy to this drug or other alpha\-adrenergic drugs
  • Patients with a history of bradycardia and low blood pressure
  • Patients with coagulation disorders
  • Patients with a history of allergy to drugs used to treat ESWL
  • Patients with mental disorders, nervous disorders and skin disorders (inflammation).
  • Patients with active infection
  • Patients who are pregnant
  • Patients who have uremia

Outcomes

Primary Outcomes

Not specified

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