An interventional study of Bupivacain and Bupivacain in Opioid Consumption and Pain Postoperative, sponsored by Başakşehir Çam & Sakura City Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-02-20.
Sponsored by Başakşehir Çam & Sakura City Hospital · Not applicable, Interventional, and Treatment
Total Hip Arthroplasty (THA) is a complex surgical procedure frequently performed to treat degenerative conditions in the hip joint. As people's life expectancy increases, the need for hip arthroplasty increases. İnvestigetors aimed to compare the analgesic properties of SIFI and QLB blocks.
5,227 studies on the registry are indexed under Pain, Postoperative; 1,154 are open to participants now.
This study's enrollment of 60 is below the median of 75 across 4,457 interventional studies indexed under Pain, Postoperative.
Browse Pain, Postoperative studies →Başakşehir Çam & Sakura City Hospital is the lead sponsor of 107 studies on the registry; 35 are open to participants now.
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Exclusion Criteria:
Group of 30 patients who underwent SIFI block
Drug: Bupivacain
Group of 30 patients who underwent QLB block
Drug: Bupivacain
Suprainguinal Fascia Iliaca Compartment block was performed with a linear probe placed over the inguinal ligament using a portable ultrasound device. After visualization of the femoral nerve, 30 ml of 0.25% bupivacaine was injected into the fascia iliaca overlying the iliopsoas muscle using an appropriate needle.
Also known as: SIFI
Quadratus Lumborum Type 3 block was performed using a portable ultrasound device with a linear probe placed between the costal margin and the iliac crest on the lateral abdominal wall. 30 ml of 0.25% bupivacaine was injected between the quadratus lumborum and psoas muscles using an appropriate needle.
Also known as: QLB Type 3
Effect on pain score
Postoperative 24-hour Visual Analog Scale was measured. ( 0=best 10=worst)
Time frame: At 1,2,4, 6, 12 and 24 hours after surgery
Opioid Consumption
Intravenous patient-controlled analgesia (PCA) with tramadol was administered to both groups in the postoperative period.
Time frame: At 1,2,4, 6, 12 and 24 hours after surgery
Plan to share: No
This study is completed, as verified in Feb 2025. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: Bupivacaine
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