A research to study the efficacy of a procedure, ultrasound guided infiltration of a local anaesthetic in abdominal muscles for providing postoperative pain relief in patient who are undergoing delivery by Caesarean Sectio
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Patients who are undergoing Caesarean Section under Spinal Anaesthesia
- Registration Number
- CTRI/2010/091/001488
- Lead Sponsor
- OT APPLICABLE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 130
Inclusion Criteria
Adult females of all Racial and Ethnic Group of child bearing age group undergoing Caesarean section under Spinal Anaesthesia with American Society of Anaesthesiology (ASA) Criteria I, IE(Emergency), II and IIE
Exclusion Criteria
Patient with history of Chronic Obstructive Pulmonary Disease, Asthma, allergic reaction to Local Aanesthetic, opioid dependence.
Patients with coagulopathy,Pre-eclampsia/eclampsia.
Patients in whom adjuvent analgesia like Paracetamol and Diclofenac is contraindicated
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Requirement of FentanylTimepoint: 24Hrs
- Secondary Outcome Measures
Name Time Method Any other complication related to Transversus Abdominis Plane Block or Intravenous PCA FentanylTimepoint: Over 24 hrs after the procedure;Mean Ramsay Sedation ScoreTimepoint: over 24 Hrs postoperatively;Mean Visual Analogue ScoreTimepoint: at the end of 12 Hrs, and 24Hrs postoperatively