Health Condition 1: O746- Other complications of spinal andepidural anesthesia during labor and delivery
Conditions
Interventions
Intervention1: Prophylactic Phenylephrine infusion: Patients will receive either 50 ml/hour of phenylephrine (Dose-0.5 �¼g/kg/min) in the intervention group intravenously,for 60-90 minutes
Control I
Sponsors
College of Medicine and Sagore Dutta Hospital Kamarhati Kolkata
Eligibility
Inclusion criteria
Inclusion criteria: a. single pregnancy at full-term (gestational age �37 weeks) b. American Society of Anesthesiologists Physical Status I and II c. aged between 20 and 35 years old undergoing caesarean section
Exclusion criteria
Exclusion criteria: a. obesity (body mass index, BMI >35 kg/m2), b. height ( 170 cm), c. active labor/ early labor d. diabetes mellitus or gestational diabetes e. hypertension or pre-eclampsia f. intrauterine growth restriction or fetal macrosomia g. placenta previa, placenta conglutination, placenta implantation h. significant co-existing maternal disease i. any absolute contraindications to spinal anesthesia such as local infection or bleeding disorders, and cases with a sensory plane block that did not reach T6 or higher.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. mean total dose of oxytocin used during CD.Timepoint: 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.proportion (%) of patients requiring a secondary uterotonic agent 2. estimated blood loss in the 24 h after surgery (EBL) 3. adverse effects during surgery (hypotension, bradycardia, nausea and vomiting, flushing, chest pain, or dyspnea). Timepoint: 24 hours | — |
Countries
India
Contacts
Public ContactDr Nairita Mayur
College of Medicine & Sagore Dutta Hospital, Kolkata
Outcome results
None listed