Goztepe Prof Dr Suleyman Yalci City Hospital
Istanbul, 34700, Turkey (Türkiye)
NCT Number: NCT07540676
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.
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Notify Me18 year–100 year
All sexes
Interventional
Not applicable
Istanbul, 34700, Turkey (Türkiye)
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Effectiveness in postoperative pain in hip surgeries
Time frame: 24 hours postoperatively
Tramadol consumption in mg
Time frame: base, 8., 6., and 24. hour postoperatively
0: no pain, 10: the worst pain
Time frame: within 24 hours postoperatively
paracetamol/nonsteroidal antiinflamatory drugs in mg
Istanbul Medeniyet University
Other
The Effect of the Quadro-Iliac Nerve Block on Postoperative Pain in Hip Surgery
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