None listed
Conditions
Interventions
Procedure/Surgery : An anesthetic in the experimental group was injected between the psoas tendon and the pubic ramus with a mixture of 20 ml of ropivacaine and 10 ml of normal saine while watching ul
Sponsors
Chungnam National University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Men and women over 18 years of age 2) Patients who underwent total hip arthroplasty under the diagnosis of arthritis after the IRB approval date 3) Patients who have completed the survey among patients admitted to the hospital for more than 48 hours after surgery
Exclusion criteria
Exclusion criteria: 1) Patients who were hospitalized for more than 48 hours after surgery and did not faithfully participate in the survey, or were discharged within 48 hours unplanned and failed to complete the survey 2) Patients who have undergone total hip arthroplasty due to reoperation, infectious disease, or fracture rather than simple total hip arthroplasty. 3) Patients with side effects related to nerve group blockage before surgery or periarticular capsule injection during surgery 4) Patients with diseases such as delirium/dementia are excluded 5) If the patient does not agree to participate in the test
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Statistically analyzed whether there was a significant difference in the degree of pain reduction between the experimental group and the control group. | — |
Secondary
| Measure | Time frame |
|---|---|
| Statistical analysis was made to see if there was a significant difference in the quality of recovery between the experimental group and the control group, and whether the shortening of hospitalization period accordingly occurred. | — |
Countries
Korea, Republic of
Contacts
Public ContactJeong Kil Lee
Chungnam National University Sejong Hospital
Outcome results
None listed