Anaesthesia
Conditions
Interventions
placebo
Sponsors
kafrelsheikh university hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Age from 20 to 60 years old. ? Both genders. ? American Society of Anesthesiologists (ASA) physical status I-II. ? Body mass index (BMI) >35 kg/m2
Exclusion criteria
Exclusion criteria: Patients with known allergies to ibuprofen and NSAIDs. ? Patients with Congestive heart failure. ? Patients with diabetes (uncontrolled) or with diabetic neuropathy. ? Patients with history of chronic pain or chronic opioid consumption. ? Patients with hepatic or renal impairment. ? Patients with bleeding diathesis with a history or risk of intracranial hemorrhage. ? Patients with gastrointestinal tract problems such as gastritis or gastric bleeding. ? Surgical procedure more than 4 hours.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary aim is evaluating the analgesic efficacy and patient recovery characteristics when utilizing opioid- free anesthesia (OFA) as part of a multimodal enhanced recovery after surgery pathway (ERAS) for morbid obese patient surgery.. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary aim of the study was to evaluate and record: ? 24-h opioid consumption. ? Patient's satisfaction. ? Adverse events. | — |
Countries
Egypt
Contacts
Public ContactAya Mohamed
Anesthesiology Faculty of Medicine Kafrelsheikh University Egypt
Outcome results
None listed