Comparative evaluation of propofol-fentanyl, propofol-midazolam and propofol-dexmedetomidine on haemodynamic and postoperative recovery for endoscopic retrograde cholangiopancreatography: A prospective, randomized controlled study

Apollo Hospitals Bilaspur0 sites93 target enrollmentTBD

ConditionsHealth Condition 1: null- ASA grade I or III patient, Non diabetic, Non hypertensive and require Endoscopic retrograde cholangiopancreatography

Overview

Phase: Phase 4
Intervention: Not specified
Conditions: Health Condition 1: null- ASA grade I or III patient, Non diabetic, Non hypertensive and require Endoscopic retrograde cholangiopancreatography
Sponsor: Apollo Hospitals Bilaspur
Enrollment: 93
Status: Completed
Last Updated: 4 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

4 years ago

Study Type

Interventional

Investigators

Sponsor

Apollo Hospitals Bilaspur

Eligibility Criteria

Inclusion Criteria

•ASA grade I and III

Exclusion Criteria

•1\.Patients with known sensitivity to study drugs
•2\.History of drug or alcohol abuse,
•3\.Morbid obesity (body mass index \>40\),
•4\.History of chronic pain or daily intake of analgesics
•5\.Oral anticoagulant use (warfarin)
•6\.Patients with bleeding diathesis
•7\.Impaired kidney or endocrinal functions
•8\.Pregnant patients and
•9\.Psychiatric patients

Outcomes

Primary Outcomes

Not specified

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