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Comparison of transdermal ketoprofen patch and transdermal fentanyl patch for pain management in patients undergone caesarean section.

Phase 2
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
ot 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
NameTimeMethod
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
NameTimeMethod
Complications like nausea, vomiting, pruritis, erythema and respiratory depression are low in Group A.Timepoint: 2hr, 4hr, 8hr, 12hr, 16, 10hr, 24hr.
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