The Effectiveness of Quadro İliac Plane Block in Percutaneous Nephrolithotomies
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorCumhuriyet University
About this trial
Our aim was to investigate the effect of quadro iliac plane block on postoperative analgesia in patients undergoing percutaneous nephrolithotomy surgery and to determine which areas of the skin this block anesthetizes.
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
Treatment groups
60 Participants
are divided into 2 treatment groupsGroup A: Control groupNo intervention 0 interventions
Group B: Quadro-İliac Plane Block(QİPB)Active comparator 1 intervention
Trial outcomes
Primary outcomes
1
Numeric Rating Scale (NRS) Scores
Description: 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
Dermatome Area
Time frame
Postoperative 2 hours2
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