Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1 ASA grade-I and II 2 Women in labour scheduled for normal vaginal delivery those seeking pain relief 3 Cephalic presentation 4 more than 34week gestation 5 Who are willing to give consent
Exclusion criteria
Exclusion criteria: 1 ASA grade- III, IV, V 2 Participants unwilling to provide consent 3 Women with Severe pre-eclampsia with coagulopathy (INR more than 1.5, platelet count less than 75,000) 4 Cephalo-pelvic disproportion (CPD) 5 Participants with known history of drug allergy to bupivacaine or dexamethasone
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Score (NRS) Timepoint: At 30 min and then every 1h till 6h post delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| Heart Rate Timepoint: At 30 min and then every 1 h till 6 h post delivery;Non invasive blood pressureTimepoint: At 30 min and then every 1h till 6h post delivery;Motor power in lower limbTimepoint: At 30 min and then every 1h till 6h post delivery;Outcome of labourTimepoint: ;APGAR scoreTimepoint: At 1 min and 5 min post delivery;Sensory levelTimepoint: at 1 hour after the first bolus at the time of top up (rescue analgesia) | — |
Countries
India
Contacts
AIIMS Rishikesh