Health Condition 1: null- pregnant women with uncomplicated pregnancy, with no cpd
Conditions
Interventions
Intervention1: Levobupivacaine: 0.1% Inj. levobupivacaine 10ml along with Inj. fentanyl 2mcg/ml bolus through epidural catheter- the epidural bolus will be given whenever patients Visual Analogue Scal
Sponsors
no
Eligibility
Inclusion criteria
Inclusion criteria: Primigravida with singleton pregnancy Willing to involve in this study Categorized under ASA PS I & II
Exclusion criteria
Exclusion criteria: Patient refusal High risk pregnancy Primigravida with CPD With fetal anomaly Allergic to local anaesthetics Injection site infection Spine abnormalities Significant coagulopathies
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Onset of analgesia 2. Duration of analgesia 3. Quality of analgesia 4. Degree of motor blockade Timepoint: 1.The onset of analgesia is -time from the first dose of epidural bolus to achieving Visual Analogue scale less than 3. 2. Duration of analgesia-onset of analgesia to patient complaint visual analogue scale more than 3. 15 min after adequate analgesia is achieved 3. quality of analgesia will be assessed by verbal scoring system 4.Presence of any motor blockade will be assessed using a Modified Bromage score | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Hemodynamic ( SpO2, MAP, PR, FHR) 2. Foetal outcome 3. Maternal satisfaction 4. Side-effects Timepoint: 1.hemodynamics every ten minutes throughout the study 2.APGAR Score at 2min and 5 min after baby delivery 3.maternal satisfaction- at the end of the study 4.side0effects throughout the study | — |
Countries
India
Contacts
Public ContactSenthil kumar T
MAHATMA GANDHI MEDICAL COLLEGE AND RESEARCH INSTITUTE
Outcome results
None listed