None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ï?? Informed written consent for participation in study. ï?? Age: 20-35 years ï?? Gender: Antenatal female patients scheduled for elective or non urgent lower segment cesarean section. ï?? ASA physical status I and II. ï?? Patients refusing consent.
Exclusion criteria
Exclusion criteria: 1.Contraindications to Spinal Anaesthesia like, Local infection or sepsis at the site of Lumbar puncture Bleeding disorders, thrombocytopenia Space occupying lesions of the brain Anatomical disorders of the spine Hypovolaemia e.g. following massive haemorrhage 2.Allergy to local anaesthetic drugs and NSAIDS. 3.Patient on any form of analgesics therapy. 4.BMI >= 25 kg/m2
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare efficacy and safety of bupivacaine and ropivacaine for post operative pain relief in lower segment cesarean section with Visual Analogue Score and total dose of rescue analgesia.Timepoint: 1st day of lower cesarean section(First 24 hours after lower segment cesarean section) | — |
Secondary
| Measure | Time frame |
|---|---|
| Effect on hemodynamic variables like Heart Rate (HR), Mean Arterial Pressure (MAP), Oxygen saturation (SpO2). Side effects & Complications if any. Timepoint: 1st day of lower segment cesarean section (24 hours of lower segment cesarean section) | — |
Countries
India
Contacts
Government Medical College, Bhavnagar.