Elective abdominal surgery patients. Surgical follow-up care, unspecified
Conditions
Interventions
Intervention 1: First intervention group: 500 mg oral acetaminophen. Treatment method, we have used multimodal treatment in this study. Prescribing pain medication before surgery is one of the natural
Sponsors
Oroumia University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients over 18 years old Volunteer
Exclusion criteria
Exclusion criteria: history of seizures History of upper gastrointestinal bleeding related to previous NSAID treatment kidney deficiency ( cr >1.6) History of alcohol, opioid Use of NSAIDs or acetaminophen within the last 24 hours Allergy to study drugs (tramadol or acetaminophen)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduce the postoperative pain _ Numeric rating scale (NRS). Timepoint: Pain intensity will be assessed as mild (NRS: 0-3), moderate (NRS: 4-6) and severe (NRS: 7-10). The NRS score during recovery is recorded at 2, 4, 6, 8, 12, and 24 hours after the patient fully wakes up from anesthesia. Method of measurement: Patient date and Numerical Pain Rating Scale (NRS) questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausea and vomiting and other complication. Timepoint: From the end of the operation until the patient feels nausea and vomiting and other complication. Method of measurement: Patient reports and observations and records of patient data. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAli Akbar Nasiri
Oroumia University of Medical Sciences
Outcome results
None listed