Pain relief during labour pai
Phase 3
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2024/02/062192
- Lead Sponsor
- Commandant
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Nulliparous gravida with a singleton pregnancy, term gestation, cephalic presentation, in the active first stage of labour
2. Cervical dilatation > 3com and <5cm
3. ASA II
4. Height >145cm
Exclusion Criteria
1. Unwilling patients
2. Multi gravida
3. Medical disorders and pregnancy associated disorders with ASA III and IV
4. Spine abnormalities and local skin infections
5. Coagulopathies
6. CPD
7. Preterm gestation
8. Non-reassuring NST
9. Preeclampsia
10. Multiple gestations
11. Breech presentation
12. Previous caesarean section
13. Known history of allergy to local anesthetics and/or fentanyl
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Onset of analgesia <br/ ><br>2. Duration of analgesia <br/ ><br>3. Quality of analgesia <br/ ><br>4. Motor blockade <br/ ><br>5. Adverse effects- hypotension, urinary retention, pruritis <br/ ><br>6. Rate of LSCSTimepoint: Initial pain assessment- Visual pain analogue score at 0 min, 5 min, 10min, 30 min, 1hr , then every 30 mins till delivery of baby
- Secondary Outcome Measures
Name Time Method eonatal parameter: OutcomeTimepoint: Fetal heart rate <br/ ><br>APGAR SCORE at 1min <br/ ><br> & 5 mins