Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Intervention1: ketamine: Inj ketamine 0.2mg/kg/hr iv infusion till baby delivery
Control Intervention1: Normal saline: Normal saline infusion 5ml/hr iv till baby delivery
Sponsors
SRM Medical college hospital
Eligibility
Inclusion criteria
Inclusion criteria: All consenting primigravidae having normal vaginal delivery, assessed under ASA 1 and 2, weight between 50 to 100kgs, height more than 150cm and less than 180cm, singleton pregnancy with cephalic presentation with 3cm cervical dilatation after obstetricians approval.
Exclusion criteria
Exclusion criteria: patients who refuse to participate in the study, patients with epilepsy,hyperthyroidism,liver, cardiac,renal disease, coagulation abnormalities and contraindications to epidural anaesthesia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To study the VAS score during second stage of labourTimepoint: Pain will be assessed by visual analogue scale every 30 minutes during labour and continued for 1 hour after baby delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. changes in haemodynamic parameters 2. APGAR score 3. Frequency of adverse effectsTimepoint: 1. The heart rate, mean arterial pressure and oxygen saturation will be monitored continuously and recorded every 30 min during the second stage of labour. 2. The APGAR score at 1 minute and 5 minutes will be recorded. 3.Adverse effects will be noted and graded according to severity. | — |
Countries
India
Contacts
Public ContactRajagopalan Venkatraman
SRM medical college hospital and research centre
Outcome results
None listed