None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All consenting parturients of the American society of anaesthesiologists, grade1 and 2 having uncomplicated cephalic singleton pregnancy and desirous of having a labour epidural
Exclusion criteria
Exclusion criteria: Hypersensitivity to study drugs, bleeding disorders, decreased platelet counts, sepsis, spinal column deformities, history of spine surgery and if parturient delivers before administering the second bolus dose.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assessment of duration of adequate analgesia with each bolusTimepoint: Till delivery of baby | — |
Secondary
| Measure | Time frame |
|---|---|
| onset of analgesia, incidence of sedation, pruritus, instrumental delivery, conversion to caesarean section and fetal outcomes like bradycardia, fetal acidosis and Apgar.Timepoint: Till delivery of baby | — |
Countries
India
Contacts
Amrita Institute of Medical Sciences