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Clinical Trials/CTRI/2024/04/064971
CTRI/2024/04/064971
Not yet recruiting
Phase 4

Comparison of efficacy of transdermal fentanyl and buprenorphine patch in post operative pain management in radical hysterectomy patients - NI

Himalayan Institute of Medical Sciences, Swami Rama Himalayan University0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: O- Medical and Surgical

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: O- Medical and Surgical
Sponsor
Himalayan Institute of Medical Sciences, Swami Rama Himalayan University
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Himalayan Institute of Medical Sciences, Swami Rama Himalayan University

Eligibility Criteria

Inclusion Criteria

  • •Age 18 to 60 years. Female patients. Patients undergoing radical abdominal hysterectomy. Written informed consent by patients. Grades 1 and 2 of the American Society of Anesthesia physical status.

Exclusion Criteria

  • •1\.Pregnant females.
  • •2\.Patients with history of pre\-existing lung and cardiac disease.
  • •3\.Patients with impaired kidney or liver function.
  • •4\.Patients who have experienced an upper respiratory illness in the prior four weeks.
  • •5\.Patients with history of smoking, respiratory or gastrointestinal infection.
  • •6\.Patients with history of any allergy to any study drug.
  • •7\.Patients on antiepileptics or antidepressants, NSAIDS, or any type of pain medicine for longer than three months.
  • •8\.Patients with any syndrome of chronic pain.
  • •9\.Inability to understand pain assessment.

Outcomes

Primary Outcomes

Not specified

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