MedPath

Post operative pain relief using Buprenorphine and Ketorolac

Not yet recruiting
Conditions
Acute appendicitis with localizedperitonitis, (2) ICD-10 Condition: K400||Bilateral inguinal hernia, with obstruction, without gangrene, (3) ICD-10 Condition: K811||Chronic cholecystitis,
Registration Number
CTRI/2023/11/059855
Lead Sponsor
Kameshwar ownself
Brief Summary

Pain is a major post-operative complication worldwide, which impairs normal body performance andincreases post-operative morbidity, hospitalization and susceptibility to infections which also can lead tochronic pain development.To compare the analgesicpotential of Buprenorphine and Ketorolac for postoperative pain relief.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
140
Inclusion Criteria

1.ASA I or II 2.Patients scheduled for elective abdomen surgeries under general anesthesia 3.Age: 20-60 years.

Exclusion Criteria
  • 1.Patient refusal.
  • 2.Allergy or hypersensitivity to Buprenorphine and Ketorolac.
  • 3.Pregnant and Lactating women 4.Patient having a.
  • Uncontrolled hypertension/diabetes mellitus.
  • History of chronic pain.
  • Psychiatric disease.
  • Alcohol or drug usage.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
2.Time duration needed for the usage of rescue analgesicBaseline ( before the surgery), | Intra operative period, | Immediate post operative period-0 minutes | 1 hour after post operative period, | 2 hours after post operative period, | 4 hours after post operative period, | 6 hours after post operative period, | 8 hours after post operative period, | 12 hours after post operative period.
1.Dose of the study drugBaseline ( before the surgery), | Intra operative period, | Immediate post operative period-0 minutes | 1 hour after post operative period, | 2 hours after post operative period, | 4 hours after post operative period, | 6 hours after post operative period, | 8 hours after post operative period, | 12 hours after post operative period.
Secondary Outcome Measures
NameTimeMethod
Time duration for rescue analgesicAt the end of surgery 0 hours,

Trial Locations

Locations (1)

Sri Muthukumaran Medical College Hospital and Research Institute

🇮🇳

Chennai, TAMIL NADU, India

Sri Muthukumaran Medical College Hospital and Research Institute
🇮🇳Chennai, TAMIL NADU, India
Kameshwar
Principal investigator
9176191069
speak2kamesh@gmail.com

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.