Hip Surgeries
Conditions
Brief summary
In this single-center retrospective study, patients who underwent hip surgery between May 2025 and November 2025, with American Society of Anesthesiology (ASA) physical status I-III, aged 18 years and older, were screened. Patients who did not undergo a block for postoperative analgesia and who used patient-controlled analgesia were included in the control group. Patients who underwent QIPB and used patient-controlled analgesia were included in the block group. Patients' postoperative tramadol consumption, pain scores assessed using the Numerical Rating Scale, and rescue analgesia requirements were recorded. The primary endpoint was total opioid consumption over 24 hours, and the secondary endpoints were postoperative pain scores and rescue analgesia requirements.
Interventions
Effectiveness in postoperative pain in hip surgeries
Sponsors
Istanbul Medeniyet University
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No
Inclusion criteria
* ASA score I-III * Underwent femoral intertrochanteric fracture or total hip replacement surgery
Exclusion criteria
* neurological deficits * mental retardation * history of alcohol or substance use
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Opioid consumption | 24 hours postoperatively | Tramadol consumption in mg |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Numeric Rating Scale | base, 8., 6., and 24. hour postoperatively | 0: no pain, 10: the worst pain |
| The Need for Rescue Analgesics | within 24 hours postoperatively | paracetamol/nonsteroidal antiinflamatory drugs in mg |
Countries
Turkey (Türkiye)
Contacts
PRINCIPAL_INVESTIGATORMesure G.N. Ozden, Ass Prof
Goztepe Prof Dr Suleyman Yalcın City Hospital
Outcome results
None listed