Health Condition 1: null- Pregnant patients undergoing Caesarean Section
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (i) Patient consented for the study (ii) ASA I or II (iii) Elective/Emergency caesarean section (iv) Full term pregnancy ( >37 weeks)
Exclusion criteria
Exclusion criteria: (i) Patient having known allergy or sensitivity to local anaesthetics (ii) Pre-eclampsia/Eclampsia (iii) Patients with cardiac or renal disease or diabetes mellitus (iv) Patients diagnosed to be having foetal distress/anomalies (v) Patients having contraindications for subarachnoid block (vi) Refusal to participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. To compare the effectiveness of prophylactic intramuscular and intravenous ephedrine in maintenance of blood pressure during caesarean section under subarachnoid block 2. To evaluate effectiveness of ephedrine in preventing intraoperative nausea and vomiting Timepoint: Intraoperative for 2 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| Degree of fetal acidosisTimepoint: After delivery | — |
Countries
India
Contacts
Bhagat Phool Singh Government Medical College for Women