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Clinical Trials/CTRI/2018/09/015839
CTRI/2018/09/015839
Completed
未知

Propofol sedation during endoscopic retrograde cholangiopancreatography: A comparison between conventional versus bispectral index guided approach and effect of diclofenac sodium along with topical pharyngeal anaesthesia.

DEPARTMENT OF ANAESTHESIA INSTITUTE OF LIVER AND BILIARY SCIENCE0 sites90 target enrollmentTBD
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
DEPARTMENT OF ANAESTHESIA INSTITUTE OF LIVER AND BILIARY SCIENCE
Enrollment
90
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
November 14, 2019
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
DEPARTMENT OF ANAESTHESIA INSTITUTE OF LIVER AND BILIARY SCIENCE

Eligibility Criteria

Inclusion Criteria

  • •ASA I \& ASA II patients between age group 18 to 65 yrs scheduled for ERCP procedure will be recruited for the study.

Exclusion Criteria

  • •Exclusion Criteria: Patients will be excluded if they have
  • •1\)Age \< 18 yrs \& \> 65 yrs
  • •2\)ASA III \& IV patients
  • •3\)Chronic Liver Disease
  • •4\)Pregnant patients
  • •5\)Patients with a history of (H/O) Drug abuse
  • •6\)Patients refusing consent
  • •7\)H/o Acute kidney injury
  • •8\)H/o allergy to propofol / lidocaine/ NSAIDS
  • •9\)Post liver transplant patients

Outcomes

Primary Outcomes

Not specified

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