Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Group BF: Received 10 mg (2ml) 0.5% hyperbaric bupivacaine with 20 microgram fentanyl: This is a Prospective study of six months duration
During the study period Patients posted for
Sponsors
Sree Balaji Medical College and Hospital
Eligibility
Inclusion criteria
Inclusion criteria: Those who consented to be part of the study and gave written consent women who are undergoing elective cesarean section for baby delivery ASA II patients.
Exclusion criteria
Exclusion criteria: ASA Grade III or Above Patients in whom spinal anesthesia was contraindicated Pre-operative hemodynamic instability, maternal heart disease, and severe anaemia History of allergy to local anaesthetic or opioids.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the onset of analgesia between the two different study groups concerning the nature of sensory block, motor block, and duration of analgesia.Timepoint: After the Administration of intrathecal local anaesthetics and opioids postoperatively, the patient is observed every 15mins 30 minutes 1 hr then every 1hr up to 24hrs | — |
Secondary
| Measure | Time frame |
|---|---|
| To find out the effectiveness and hemodynamics of the drugs. To find out the Pain score at 30 min,4hr, 8hr, 12hr post-op.Timepoint: To find out the hemodynamics changes at 1,3,5,10,15,30,45,60 minutes after spinal anaesthesia To find out the Pain score at 30 min,4hr, 8hr, 12hr post-op. | — |
Countries
India
Contacts
Public ContactDr Kala B
Sree Balaji Medical College and Hospital
Outcome results
None listed