A study to compare ROPIVACAINE AND LEVOBUPIVACAINE ALONG WITH FENTANYL FOR LABOUR PAI
Not Applicable
Completed
- Conditions
- Health Condition 1: null- pregnant women with uncomplicated pregnancy, with no cpd
- Registration Number
- CTRI/2016/01/006544
- Lead Sponsor
- no
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Primigravida with singleton pregnancy
Willing to involve in this study
Categorized under ASA PS I & II
Exclusion Criteria
Patient refusal
High risk pregnancy
Primigravida with CPD
With fetal anomaly
Allergic to local anaesthetics
Injection site infection
Spine abnormalities
Significant coagulopathies
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.Degree of motor blockade <br/ ><br>Timepoint: 1.The onset of analgesia is -time from the first dose of epidural bolus to achieving Visual Analogue scale less than 3. <br/ ><br>2. Duration of analgesia-onset of analgesia to patient complaint visual analogue scale more than 3. <br/ ><br>15 min after adequate analgesia is achieved <br/ ><br>3. quality of analgesia will be assessed by verbal scoring system <br/ ><br>4.Presence of any motor blockade will be assessed using a Modified Bromage score
- Secondary Outcome Measures
Name Time Method 1.Hemodynamic ( SpO2, MAP, PR, FHR) <br/ ><br>2.Foetal outcome <br/ ><br>3.Maternal satisfaction <br/ ><br>4.Side-effects <br/ ><br>Timepoint: 1.hemodynamics every ten minutes throughout the study <br/ ><br>2.APGAR Score at 2min and 5 min after baby delivery <br/ ><br>3.maternal satisfaction- at the end of the study <br/ ><br>4.side0effects throughout the study <br/ ><br>