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Clinical Trials/CTRI/2021/05/033653
CTRI/2021/05/033653Not yet recruitingNot Applicable

Effectiveness Of Transdermal And Epidural Fentanyl, Along With Epidural Ropivacaine On Post Operative Pain Among The Patients Undergoing Major Infra Umbilical Abdominal Surgeries: A Cross-Sectional, (Two Group) Comparative Study.

Dept Of Anaesthesiology and Critical Care1 site in 1 country42 target enrollmentStarted: May 24, 2021Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
42
Locations
1
Primary Endpoint
To compare the post-operative pain scores in patients receiving transdermal and epidural fentanyl

Study Overview

Brief Summary

post operative analgesia is important for early postoperative recovery. In this study, I am comparing two different routes of administration of fentayl. ie, transdermal and epidural routes, in patients undergoing major infra umbilical abdominal surgeries.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Age between 18-60 years
  • Body mass index
  • Laparotomy with below umbilicus incision.

Exclusion Criteria

  • Known allergy to the study drug
  • Contraindication to neuraxial blockade
  • Patients with cognitive impairment
  • Uncontrolled cardiovascular / hepatic / renal disease or impaired pulmonary function.
  • Patients having intolerance to opioid
  • Pregnant and breastfeeding females.

Outcomes

Primary Outcomes

To compare the post-operative pain scores in patients receiving transdermal and epidural fentanyl

Time Frame: 24 hours postoperatively

Secondary Outcomes

  • To compare the adverse events in patients receiving transdermal and epidural fentanyl(24 hours postoperatively)

Investigators

Sponsor
Dept Of Anaesthesiology and Critical Care
Sponsor Class
Private medical college

Study Sites (1)

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