Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Drug: Intravenous Ibuprofen
Drug: Intravenous Paracetamol: Intervention 1 (Group I): Intravenous Ibuprofen 800mg , 8 hourly
Intervention 2 (Group P): Intravenous Paracetamol 1g, 8 hour
Sponsors
GMERS Medical College and Hospital Gotri Vadodara
Eligibility
Inclusion criteria
Inclusion criteria: Female patient posted for Vaginal hysterectomy under Spinal anesthesia consenting for participating in this study Patient aged between 35-65 years All elective surgeries of ASA I and II patients
Exclusion criteria
Exclusion criteria: 1.Patient s refusal 2.History of allergy or hypersensitivity to NSAIDs 3.History of Peptic ulcer or intestinal Inflammatory disease. 4.Contraindications for spinal anaesthesia 5.Coagulation disorders 6.Any systemic organ involvement or any other co morbidity. 7.Duration of Surgery more than 2 hours
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total opioid consumption in 24 hours with use of two study drugsTimepoint: Total opioid consumption in 24 hours with use of two study drugs | — |
Secondary
| Measure | Time frame |
|---|---|
| To Compare the duration of analgesia with either of the study drug (from first administration to requirement of rescue analgesia) To assess hemodynamic stability of both drugs To compare incidence of adverse eventsTimepoint: Immediate postoperatively, a baseline VAS observed Study drug administered 30 mins after shifting the patient to a recovery room VAS Score assessed at 30 min,60 min, 90min, 2hrs & there after every 2 hrs following the 1st dose till 24 hours | — |
Countries
India
Contacts
Public ContactDr. Pooja Zala
GMERS Medical college and Hospital, Gotri, Vadodara
Outcome results
None listed