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Clinical Trials/CTRI/2019/03/018003
CTRI/2019/03/018003
Completed
Phase 3

Comparision of the Effect Between Dexmedetomidine And Fentanyl on Median Effective Concentration (EC 50) of Propofol for I gel insertion: A Randomized Controlled Trial

Ankur Luthra0 sites0 target enrollmentTBD
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Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Ankur Luthra
Status
Completed
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\.American Society of Anesthesiologists physical status I or II
  • •2\.Age of 20ââ?¬â??60 years
  • •3\.Either gender
  • •4\.Estimated operation time of ââ?°Â¤ 2 hours and anaesthesia time of ââ?°Â¤ 3 hours
  • •5\.Written informed consent to undergo the therapeutic regimen

Exclusion Criteria

  • •1\.Renal dysfunction (serum creatinine \> 1\.2mg/dl)
  • •2\.Liver dysfunction (liver enzymes twice the normal range or higher)
  • •3\.History of chronic use of sedatives/ narcotics or analgesics/Beta blockers
  • •4\.BMI more than 30 kg/m2 or less than 15 kg/m2
  • •5\.Allergy to study medication

Outcomes

Primary Outcomes

Not specified

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