Health Condition 1: O82- Encounter for cesarean delivery without indication
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Patients undergoing elective lower segment caesarean section 2)American Society of Anaesthesiologists (ASA) Grade II
Exclusion criteria
Exclusion criteria: 1)Patients not willing to participate in the study 2)Patients with pre-existing or pregnancy-induced hypertension, diabetes mellitus, known cardiovascular or cerebrovascular disease. 3)Patients with fetal abnormalities. 4)Patients indicated for LSCS i/v/o fetal distress. 5)Patients with any known hypersensitivity to any of the study drug. 6)Patients contraindicated to central neuraxial blocks
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the effect on neonatal cord blood PH after the administration of bolus doses of Ephedrine and Phenylephrine.Timepoint: Intraoperative duration | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To compare maternal blood pressure and heart rate with administration of bolus doses of Ephedrine and Phenylephrine. 2)To compare effects on neonatal cord blood glucose levels after administration of bolus doses of Ephedrine and Phenylephrine. Timepoint: Intraoperative duration | — |
Countries
India
Contacts
Bharati Vidyapeeth Deemed to be University Medical College