Comparison of transdermal ketoprofen patch and transdermal fentanyl patch for pain management in patients undergone caesarean section.
Phase 2
Not yet recruiting
- Conditions
- Health Condition 1: O754- Other complications of obstetric surgery and procedures
- Registration Number
- CTRI/2024/02/062335
- Lead Sponsor
- Dr. D. Y. Patil medical college, hospital and research centre.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Ages between 18-40 years scheduled for elective and emergency caesarean sections.
2)ASA grade I and II fit parturient women.
3)Body mass index (BMI) between 20-25kg/m2.
4)Acceptance of study and signing informed consent.
Exclusion Criteria
1)Denial to consent for the study
2)History of NSAIDs allergy and opioid sensitivity.
3)History of opioid abuse.
4)Active peptic ulcer disease within 6 months
5)Major systemic illness like Bronchial Asthma, Epilepsy, COPD, Liver disease, Cardiac disease, Renal disease and Coagulopathy.
6)Contraindications to spinal anaesthesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Verbal Assessment Score(VAS) is lower in Group A. Sedation is low in Group A when compared to Group B.Timepoint: 2hr, 4hr, 8hr, 12hr, 16, 10hr, 24hr.
- Secondary Outcome Measures
Name Time Method Complications like nausea, vomiting, pruritis, erythema and respiratory depression are low in Group A.Timepoint: 2hr, 4hr, 8hr, 12hr, 16, 10hr, 24hr.