None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Pregnant patients with ASA I and II 2)Patients scheduled for elective caesarean section
Exclusion criteria
Exclusion criteria: 1)Patient refusal to participate in the study 2)History of allergy to any of the study drug 3)Multiple gestation 4)Patients in whom spinal anaesthesia is contraindicated (spinal abnormalities, infection at the site of injection, coagulopathies, raised intracranial tension)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Time to first post operative analgesic requirement (Total duration of analgesia) 2.To assess the onset and total duration of sensory and motor blockadeTimepoint: Intra operative and 6 hours in post operative period | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.To assess the hemodynamic parameters 2.To assess the patient satisfaction level 3.To assess the surgeon satisfaction level 4.To note any adverse effectsTimepoint: Intra operative and 6 hours in post operative period | — |
Countries
India
Contacts
All India Institute of Medical Sciences, New delhi