Comparison of two different low concentrations of Ropivacaine for labor epidural analgesia
Not Applicable
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2022/05/042543
- Lead Sponsor
- Sardar Patel Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
a singleton fetus in cephalic presentation at term ( >37 weeks gestation) belonging to ASA class 2 who requested epidural analgesia with no contraindication to epidural catheterization were selected and randomly divided into two groups.
Exclusion Criteria
1.Patients not giving consent
2.BMI >35kg/m2
3.Gestation diabetes
4.Hypertensive disorders
5.Premature Rupture of membranes
6.Coagulation disorder
7.Infection at the site of epidural prick
8.Past history of any drug reaction
9.Patients having psychiatric illness
10.Neurological deficits.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare duration of analgesiaTimepoint: Upto delivery of parturient
- Secondary Outcome Measures
Name Time Method 1.Onset of analgesia <br/ ><br>2.Quality of analgesia (VAS) <br/ ><br>3.No. of episodes of breakthrough pains <br/ ><br>4.Duration of Labour <br/ ><br>5.Incidence of motor block (Breen Modified Bromage Score) <br/ ><br>6.Time from Epidural to Delivery <br/ ><br>7.Foetal side effects <br/ ><br>8.Parturient satisfaction <br/ ><br> <br/ ><br> <br/ ><br>Timepoint: upto 30 minutes after delivery of parturient