cholecystitis. cholecystitis
Conditions
Interventions
Intervention 1: The first Intervention group will receive a pain pump containing Fentanyl 100 ml and then intravenous Ketorolac 30 mg at intervals of zero, 8 and 16 hours after surgery. Intervention 2
Sponsors
Ardabil University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients who are undergoing laparoscopic cholecystectomy surgery at Imam Khomeini Hospital in Ardebil. Being at the age of 20 and 60 years old Patients who accept to participate in the research.
Exclusion criteria
Exclusion criteria: Pregnancy History of Asthma and Pulmunary disease History of heart disease History of CKD (chronic kidney disease) or dialysis History of GI (Gastrointestinal) bleeding History of HTN (hypertension) History of Anemia Using Warfarin Consumers simultaneously ACEI (angiotensin converting enzyme inhibitor) and Furosemide Drug dependence Allergic reaction to ibuprofen or NSAIDS or celecoxib
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Abdominal pain. Timepoint: 6,12 ,18, 24 hours after the operation, pain will be evaluated. Method of measurement: The assessment of abdominal pain is based on the Visual Analogue Scale system.;Shoulder pain. Timepoint: 6,12,18,24 hours after surgery. Method of measurement: The assessment of pain is based on the Visual Analogue Scale system.;Nausea and Vomiting. Timepoint: 6,12,18,24 hours after surgery. Method of measurement: The assessment is based on the N/V(Nausea and Vomiting)system.;Loss of consciousness. Timepoint: 6,12,18,24 hours after surgery. Method of measurement: The assessment is based on the Ramsay score. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSomaye Hoghughi
Ardabil University of Medical Sciences
Outcome results
None listed