Health Condition 1: O82- Encounter for cesarean delivery without indication
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Parturients who give written informed consent. 2. ASA physical status classes I and II) 3. Age between 19- 35 years 4. Primigravida or multigravida undergoing lower segment caesarean section for the first time. 5. Parturients with uncomplicated full term singleton pregnancy
Exclusion criteria
Exclusion criteria: 1. Parturients refusing to participate in the study . 2. ASA physical class >II 3. Parturients with height 4. Parturients with (1) Hypertensive disorders of pregnancy , essential hypertension (2) Anaemia, (3) previous abdominal surgeries, (4) diabetes mellitus, (5) Cardiac disease (8) Abruptio placenta, placenta previa (9) features of increased intracranial pressure 5. Any contraindication to spinal anaesthesia, 6. Known allergy to ketamine or local anaesthetics .
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to assess the effect of single low dose of ketamine intravenously in cesarean section under spinal anaesthesia after delivery of the baby in reducing the incidence of breakthrough pain postoperativelyTimepoint: Pain assessed every 30 min for 6 hrs post caeserean section. | — |
Secondary
| Measure | Time frame |
|---|---|
| the possibility of prolongation of duration of spinal anaesthesia .Timepoint: Duration of sensory and motor blockade assessed every 30 min post operatively till 6hrs post caeserean section. | — |
Countries
India
Contacts
Bangalore medical college and research institute