Comparison of QIPB and SIFICB in Hip Surgery
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-99
SponsorCumhuriyet University
About this trial
The aim is to compare the postoperative analgesic effects of Quadroiliac Plane Block (QIPB) and Suprainguinal Fascia Iliaca Compartment Block (SIFICB) in patients undergoing hip surgery.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult patients over 18 years of age who underwent percutaneous nephrolithotomy under general anesthesia and were I-II-III according to the American Society of Anesthesiologists (ASA) risk classification were included in the study.
Disqualifiers
patients who did not give consent,
patients with coagulopathy,
patients with signs of infection at the block application site,
patients using anticoagulants,
Trial design
Design model
Parallel
Treatments tested in this trial
Quadro-İliac Plane Block(QİPB)
Procedure/Surgery40 mL of 0.25% bupivacaine
Suprainguinal Fascia Iliaca Compartiment Block
Procedure/Surgery30 mL of 0.25% bupivacaine
Treatment groups
60 Participants
are divided into 2 treatment groupsGroup A: Quadro-İliac Plane Block(QİPB)Active comparator 1 intervention
Group B: Suprainguinal Fascia Iliaca Compartiment Block (SIFICB)Active comparator 1 intervention
Trial outcomes
Primary outcomes
1
Numeric Rating Scale (NRS) Scores
Numerical rating scale is used for pain assessment. The scores of the numerical rating scale changes between 0 to 10 points. 10 points mean "the most severe pain that the patient ever had". 0 point means "there is no pain." Higher scores mean worse outcome.
Time frame
Postoperative 24 hoursSecondary outcomes
1
Total tramadol consumption
Postoperative total analgesic need was recorded as "milligram" in unit.
Time frame
Postoperative 24 hoursSponsors and contacts
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Source ClinicalTrials.gov
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