Pain after surgery. Other acute postprocedural pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who are candidates for lumbar disc herniation surgery Having informed consent to participate in the study Surgery performed by a surgeon
Exclusion criteria
Exclusion criteria: Having a history of systemic kidney, liver, cardiovascular disease, high blood pressure, diabetes, or malignancy Having a history of chronic opioid or painkiller use, and no known allergies to the study drugs or seasonal allergies
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Propofol dosage. Timepoint: After the intervention. Method of measurement: Operating room sheet.;Pain intensity. Timepoint: In the recovery room and at 2, 6, 12, and 24 hours after surgery. Method of measurement: Visual analog scale.;Ramsey Score. Timepoint: In recovery, 2, 4, 6, 12, 24 hours after surgery. Method of measurement: By registering the Ramsey Score. | — |
Secondary
| Measure | Time frame |
|---|---|
| Mean arterial pressure. Timepoint: At the beginning of surgery and every 15 minutes until the end of surgery, during recovery, and two and four hours after surgery. Method of measurement: Cardiac monitoring.;Mean arterial pressure. Timepoint: At the beginning of surgery and every 15 minutes until the end of surgery, during recovery, and two and four hours after surgery. Method of measurement: Cardiac monitoring.;Arterial oxygen saturation. Timepoint: At the beginning of surgery and every 15 minutes until the end of surgery, during recovery, and two and four hours after surgery. Method of measurement: Cardiac monitoring. | — |
Countries
Iran (Islamic Republic of)
Contacts
Arak University of Medical Sciences