Health Condition 1: N00-N99- Diseases of the genitourinary system
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. ASA grade 1 or 2 fit patients. 2. Patients undergoing abdominal hysterectomy. 3. Haemodynamically stable patients with all investigations within normal limits. 4. Written informed consents from concerned patients.
Exclusion criteria
Exclusion criteria: 1. Patients not willing to participate in study 2. Patients with ASA grade 3 and above 3. Patients aged less than 30 and more than 60 years. 4. Patients posted for emergency procedures. 5. Patients with known allergy to the study drugs. 6. Patients with difficult intubation. 7. Patients with psychiatric conditions, coagulopathies, naurological, neuromuscular or cardiovascular disease or impairment of hepatic or renal function. 8. Patients with coagulopathies and contraindications to spinal anaesthesia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the analgesic effect of Intravenous Ibuprofen versus Intravenous Paracetamol as post operative analgesia in patients who have undergone abdominal hysterectomy.Timepoint: After administration of intravenous analgesic, comparison between 2 groups of efficacy and duration of action by monitoring VAS scores at 0,2,4,6,8,12,24,48 hours respectively. | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the analgesic effect of Intravenous Ibuprofen versus Intravenous Paracetamol as post operative analgesia in patients who have undergone abdominal hysterectomy.Timepoint: At baseline, 2 hrs, 4 hrs, 6 hrs, 8 hrs, 12 hrs, 24 hrs & 48 hrs after administration of medication | — |
Countries
India
Contacts
Dr. DY Patil Medical College, Hospital and Research Centre, Pimpri, Pune