Health Condition 1: O82- Encounter for cesarean delivery without indication
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 60 antenatal women term gestation with no comorbidities undergoing Caesarean section belonging to ASA 2 will be randomly allocated into 2 groups of 30 each Group P will receive percutaneous stimulation of auricular pressure points with a stimulation device attached at the end of caesarean procedure and Group C will be control group
Exclusion criteria
Exclusion criteria: Pregnant women ASA 3 and above with comorbid illnesses such as hypertension, diabetes mellitus, cardiac/renal/liver disease, BMI >35, presence of pacemakers and biomedical implants, patients with altered mental status
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To provide efficacious analgesia and to overcome adverse effects of opioidsTimepoint: 24 to 48 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative pain score using VAS scoring, need for rescue analgesics,dose required in 48 hours,postoperative nausea and vomitingTimepoint: Secondary outcomes assessed in first 48 hours postoperatively | — |
Countries
India
Contacts
Madras Medical College