Comparison of two techniques for labor analgesia using levobupivacaine-fentanyl
Phase 4
- Conditions
- Health Condition 1: 1- Obstetrics
- Registration Number
- CTRI/2024/04/066268
- Lead Sponsor
- niversity college of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Nulliparous pregnant females with singleton pregnancy with vertex presentation, gestation age more than 37 weeks, cervical dilation 2 to 5 cm
Exclusion Criteria
Preeclampsia or gestational hypertension, pre existing gestational diabetes, contraindication to neuraxial anaesthesia, history of allergy to local anaesthetics or opioids
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Block onset timeTimepoint: Once, when VAS score is 1
- Secondary Outcome Measures
Name Time Method Percentage of patients having effective block in the first 10 mins,block characteristics:sensory block level and motor block intensity,occurrence of maternal side effects to neuraxial procedure,ancillary observations:type of delivery,neonatal outcomes,patient satisfaction.Timepoint: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 60, 120, 180, 240, 300, 360 min