Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Intervention1: 0.2% ROPIVACAINE: 0.2% ROPIVACAINE WITH FENTANYL 2mcg/ml 12ml INCREMENTAL BOLUS FOLLOWED BY 10ml/hour INFUSION OF SAME CONCENTRATION.
Control Intervention1: 0.1 % ROPIVACAINE: 0.1% ROPI
Sponsors
Shimoga institute of medical sciences
Eligibility
Inclusion criteria
Inclusion criteria: 1. Singleton nulliparous pregnancy 2. Women with gestational age >36 weeks 3. Parturients in active stage of labor 4. Uncompleted pregnancy
Exclusion criteria
Exclusion criteria: 1. ASA physical status 3 or 4 2. Preterm gestation 3. Allergy to study drug 4. Patient refusal 5. Pregnancy with comorbidities like GDM, PIH and other systemic disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| ASSESSMENT OF EFFICACY OF ANALGESIA BY VAS SCORETimepoint: EVERY 10 MINUTES IN FIRST HOUR, EVERY 30 MINUTES FOR NEXT 2 HOUR AND EVERY HOUR TILL DELIVERY | — |
Secondary
| Measure | Time frame |
|---|---|
| EVALUATE TIME OF ONSET OF ANALGESIA, TOTAL DOSE OF ANAESTHETIC USED, DEGREE OF MOTOR BLOCKADE, MODE OF DELIVERY, MATERNAL SATISFACTION AND HAEMODYANAMIC PARAMETERSTimepoint: EVERY 10 MINUTES IN FIRST HOUR, EVERY 30 MINUTES FOR NEXT 2 HOUR AND EVERY HOUR TILL DELIVERY | — |
Countries
India
Contacts
Public ContactDR BHAGYALAXMI KADEWADI
SHIMOGA INSTITUTE OF MEDICAL SCIENCES
Outcome results
None listed