Health Condition 1: O82- Encounter for cesarean delivery without indication
Conditions
Interventions
Intervention1: the intra operative pain relief comparison: To determine the intraoperative pain relief, patient is given 0.5mg/kg Ketamine IV in comparison to patient receiving similar volume of NS, f
Sponsors
Maharana Bhupal Government Hospital
Eligibility
Inclusion criteria
Inclusion criteria: Parturients with Singleton pregnancy (37-42 weeks) Elective LSCS ASA Grade II
Exclusion criteria
Exclusion criteria: Patient Refusal Non cooperative Parturients Patients with medical comorbidities like, cardiac diseases such as inadequate left ventricular ejection fraction (Ejection Fraction less than 45%), valvular or ischaemic heart disease, uncontrolled hypertension, heart blocks, arrhythmia, cardiac failure, uncontrolled diabetes mellitus, hepatic, renal, endocrine, haematological, autoimmune, psychiatric, neurological diseases, neuromuscular diseases, bronchial asthma, chronic obstructive pulmonary disease. Allergy to study drug - Ketamine Patients who participated in another study within 30 days
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To Evaluate the intra operative pain relief achieved for the patient on giving 0.5 mg/kg of Ketamine intravenously following child deliveryTimepoint: After childbirth at 0,2,5,10,15,20,30 mins intraoperatively and at End of surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the post operative analgesic effect of low dose ketamineTimepoint: At 2,6 ,12 and 24 hours post operatively.;To look for any adverse effects/complications associated with administration of ketamineTimepoint: | — |
Countries
India
Contacts
Public ContactDr Arjun P Raj
RNT Medical College
Outcome results
None listed