anesthesiology. Acute pain, not elsewhere classified
Conditions
Interventions
Intervention 1: Intervention Group 1: This group will receive patient-controlled analgesia (PCA) via auto-infusion pump postoperatively. The PCA solution will contain 3 grams of acetaminophen, 8 milli
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Age range 18-60 years American Society of Anesthesiologists(ASA) Class I-III Having full consent to enter the study A candidate for abdominal hysterectomy
Exclusion criteria
Exclusion criteria: History of allergy to any of the drugs used in the study History of kidney or liver failure Obesity and Body mass index greater than 35 Pregnancy and lactation Addiction to any type of narcotics or substance abuse History of psychiatric or neurological disorders Uncontrolled hypertension Patients with a history of seizures Bradycardia and cardiac conduction block
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain severity. Timepoint: Upon arrival in the recovery room and at 2, 6, 12, and 24 hours after receiving pain pumps. Method of measurement: The Numerical Rating Scale (NRS).;Incidence of complications. Timepoint: Upon arrival in the recovery room and at 2, 6, 12, and 24 hours after receiving pain pumps. Method of measurement: Interview and physical examination. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient satisfaction. Timepoint: 24 hours postoperatively after receiving the pain pumps. Method of measurement: Likert Scale scoring system. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNegin Mousavi
Iran University of Medical Sciences
Outcome results
None listed