Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Intervention1: Epidural bolus of magnesium sulphate with bupivacaine infusion combined with intrathecal fentanyl: Epidural bolus of magnesium sulphate 25mg with bupivacaine 0.1% infusion combined with
Sponsors
Srinivas Institute of Medical Sciences and Research Institute
Eligibility
Inclusion criteria
Inclusion criteria: 1. Parturients in age group of 18 â?? 35yrs for planned vaginal delivery. 2. Parturients in first stage of labour with cervical dilatation greater than or equal to 3cms. 3. Parturients in height range of 145 â?? 175 cms and in weight range of 50 â?? 100 kgs.
Exclusion criteria
Exclusion criteria: 1.Pregnant patient not consenting for study. 2.History of allergy to local anesthetics. 3.Coagulation abnormality. 4.Infection at the site of the injection. 5.Any abnormality or disease of the spine. 6.Patient with any uncontrolled systemic illness. 7.Parturient with pre-eclampsia and eclampsia who received IV Magnesium for obstetric management. 8.Parturients with cardiac diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the effectiveness and quality of labour analgesia with and without epidural bolus dose of 25 mg of magnesium sulphate along with intrathecal fentanyl ( 15 mcg ) and epidural bupivacaine infusion ( 0.1 % ).Timepoint: Patients vitals parameters will be assessed at baseline, 5, 15, 30, 60, 90 and 120 min and labour pain score and fetal well being will be assessed till the delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| Hypotension, motor block, itching, nausea and vomitingTimepoint: At baseline, 5, 15, 30, 60, 90 and 120 min and till the time of delivery | — |
Countries
India
Contacts
Public ContactDr Prashanth Kumar C
Srinivas Institute of Medical Sciences and Research Centre
Outcome results
None listed