None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients from 19 to 60 years of age who underwent primary anterior cruciate ligament reconstruction at Chung-Ang University Hospital and can cooperate in collecting data
Exclusion criteria
Exclusion criteria: Patients with an American Society of Anesthesiologist grade 3 or higher A previous history of previous knee surgery or reconstruction of other ligaments Patients who underwent autogenous reconstruction of the anterior cruciate ligament, re-reconstruction of anterior cruciate ligament, or concomitant high tibial osteotomy Patients who have allergies or contraindications of medication used in this study for pain control and those who do not consent to use Patients who are constantly using analgesics regardless of the study Patients who have serious cardiovascular, kidney disease, hematologic abnormalities, obesity (BMI> 35)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual analog scale | — |
Secondary
| Measure | Time frame |
|---|---|
| pain VAS score (Visual analog scale);use of rescue medication,;side effects;patient satisfaction with pain control | — |
Countries
Korea, Republic of
Contacts
Chung-Ang Univerisity Hospital