None listed
Conditions
Interventions
Intervention1: ringer lactate solution: intravenous access will be secured, and 500 mL of ringer lactate solution will be started to preload
Control Intervention1: trict aseptic precautions, lumbar e
Sponsors
Department of Obstetrics and Gynaecology
Anaesthesiology
Eligibility
Inclusion criteria
Inclusion criteria: Age 18-30 years term pregnancy with a singleton live fetus in vertex presentation when in active stage of labor with cervical dilation of >4cm. Primigravida Patient giving written informed consent
Exclusion criteria
Exclusion criteria: â?? Patient refusal â?? Preeclampsia , Gestational diabetes â?? previous lower section cesarean section â?? multiple pregnancy â?? abnormal lie or placenta praevia and those with associated medical history like morbid obesity â?? bleeding disorders/anticoagulation therapy â?? severe anemia or any psychiatric or neurologic disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hemodynamic parameters will be monitored that is blood pressure, heart rate, oxygen saturationTimepoint: Baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| comparing the total consumption of drug, number of rescue boluses given in case of breakthrough pain(VAS3) felt by the patient ,motor bloakade by Bromage score, duration of second stage of labour, number of emergency cesarean sections, incidence of assisted/instrumental vaginal delivery and the Apgar score of neonate in each patientTimepoint: 24 hrs | — |
Countries
India
Contacts
Public ContactProf Dinesh Singh
King Georges Medical University Lucknow
Outcome results
None listed