COMPARISON OF A DRUG NAMED ROPIVACAINE AT A PARTICULAR CONCENTRATION USED WITH ADDITION OF ANOTHER DRUG NAMED FENTANYL FOR RELIEVING PAIN DURING LABOUR USING AN INJECTION AT THE BACK NAMED DURAL PUNCTURE EPIDURAL TECHNIQUE
Phase 1
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2019/09/021041
- Lead Sponsor
- Mahatma Gandhi Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Primigravida with singleton pregnancy
Exclusion Criteria
Complicated pregnancy, High risk pregnancy, CPD, Foetal anomaly, Local anaesthetics allergy, Coagulopathy, Spine abnormalities.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Objective : <br/ ><br>1. Quality of analgesia <br/ ><br>Timepoint: assessed after and in every 2 min interval from the time of injection of initial bolus of the study drug. Analgesia was considered adequate when the pain score reduced to VAS 3.
- Secondary Outcome Measures
Name Time Method Secondary Objective: <br/ ><br>1. Onset of analgesia <br/ ><br>2.Degree of motor blockade <br/ ><br>3.Duration of analgesia <br/ ><br>4.Mode of delivery <br/ ><br>5.Incidence of PDPH <br/ ><br>6.Fetal outcome by APGAR score <br/ ><br>7.Side-effects- hemodynamics, pruritis, urinary retention <br/ ><br>Timepoint: 1.Time taken from the epidural topup to decrease in VAS score3 <br/ ><br>2. Assessedd very 5-15minutes after giving the drug <br/ ><br>3. Time duration between VAS3 to VAS3 <br/ ><br>4. Instrumental / Section <br/ ><br>5. Patient complaining frontal headache on sitting after 24hrs and relieved by lying supine <br/ ><br>6. Assessed at 1minute & 5minute after child birth <br/ ><br>7. Assessed throughout the study from the time of epidural till the time of discharge.