Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Group I: Inj.Ibuprofen 400 mg IV is administered 15 min before the end of procedure for FESS and pain intensity is measured using VAS score postoperatively
Control Intervention1: Group
Sponsors
SRM Medical collage Hospital and Research centre
Eligibility
Inclusion criteria
Inclusion criteria: ASA 1 and ASA 2 Patients patient weight between 50 to 80 kg
Exclusion criteria
Exclusion criteria: Hepatic disease and renal disorders History of GERD and peptic ulcer History of drug allergy patient with coagulation abnormality
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of Post operative analgesiaTimepoint: assessment of VAS score at 0hour,4hours,8hours,12hours, 16hours,20hours and 24 hours, | — |
Secondary
| Measure | Time frame |
|---|---|
| VAS score during first 24 hrs of postoperative period Total amount of NSAID used Total amount of rescue analgesic used Timepoint: 0 to 24 hrs after the end of procedure | — |
Countries
India
Contacts
Public ContactDrR Balaji
SRM Medical college hospital and research centre
Outcome results
None listed