Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All pregnant females delivered by vaginal route requiring episiotomy ( mediolateral type)
Exclusion criteria
Exclusion criteria: Antenatal females not willing to participate in the study. 2. Allergy to local anaesthetics agents or Ropivacaine 3. Those who received epidural analgesia in labour. 4. 3rd degree perineal tear/ complete perineal tear (CPT). 5. Instrumental delivery. 6. Third stage complications like uterine inversion, PPH.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the requirement of extra analgesia in both groups upto 6 hours after episiotomyTimepoint: To compare the requirement of extra analgesia in both groups upto 6 hours after episiotomy | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To study the visual analogue scale (VAS) score immediately after suturing, 6hrs & 24 hours after episiotomy repair, comparing Lignocaine 1% & Ropivacaine 0.75% as a local anaesthetic 2. To study the satisfaction level of patients after 24 hours with Ropivacaine Vs lignocaine injection during perineal repair following vaginal birth using 5 point LIKERT scale. 3. To study any side effects of Ropivacaine & any voiding difficulties till 6 hours of episiotomy repairTimepoint: 1. VAS score (VAS) score to be seen immediately after suturing, 6hrs & 24 hours after episiotomy repair 2. satisfaction level of patients after 24 hours of repair 3. side effects of Ropivacaine & any voiding difficulties till 6 hours post repair | — |
Countries
India
Contacts
AIIMS Jodhpur