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Clinical Trials/CTRI/2018/03/012694
CTRI/2018/03/012694
Recruiting
Phase 4

Comparative evaluation of transdermal buprenorphine versus intramuscular diclofenac as postoperative analgesic for upper abdominal surgery under general anesthesia

Department of Anesthesiology0 sites0 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: null- Upper abdominal surgery under general anesthesia.
Sponsor
Department of Anesthesiology
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • ASA grade I or II.
  • Posted for elective upper abdominal surgical procedure under general anesthesia with likely duration of postoperative hospital stay more than 3 days.
  • Willing to provide written informed consent.

Exclusion Criteria

  • Women who are pregnant or breast feeding.
  • Serious concomitant disease of vital organs, including the liver.
  • Febrile patient.
  • Impaired respiratory function.
  • History of myasthenia gravis.
  • History of convulsive disorders.
  • History of delirium tremens.

Outcomes

Primary Outcomes

Not specified

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