comparison of acupressure with a drug for prevention of vomiting during delivery with operation.
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2022/08/045048
- Lead Sponsor
- Department of Anaesthesia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Age 18 to 45 years
2.ASA physical status I-II.
3.Scheduled for elective LSCS under SA.
4.Gestation � 36 weeks.
Patient refusal.
Patient with, coagulopathies or anticoagulant medication,
Systemic disease, hypothyroidism, diabetic neuropathy,
Previous history of postoperative nausea and vomiting(PONV), motion sickness,
Patients receiving any of the following drugs within 24 hr before the study : opioids, tricyclic antidepressants, droperidol, phenothiazine, metoclopramide, antacids, H2-antagonists, scopolamine, cannabinoids, antihistamines, corticosteroids or benzodiazepines
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method