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The Effectiveness of Quadro İliac Plane Block in Percutaneous Nephrolithotomies

Comparison of the Effects of Ultrasound-Guided Quadro-İliac Plane Block on Postoperative Pain Level and Analgesia Requirement in Patients Undergoing Percutaneous Nephrolithotomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07203859
Enrollment
60
Registered
2025-10-02
Start date
2025-09-25
Completion date
2026-10-01
Last updated
2026-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Percutaneous Nephrolithotomy, Postoperative Pain

Keywords

postoperative pain, regional anesthesia, percutaneous nephrolithotomy, quadroiliac plane block, opioid free analgesia, ibuprofen, novel fascial plane block

Brief summary

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.

Interventions

PROCEDUREQuadro-İliac Plane Block(QİPB)

40 mL of 0.25% bupivacaine

Sponsors

Cumhuriyet University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* patients who did not give consent, * patients with coagulopathy, * patients with signs of infection at the block application site, * patients using anticoagulants, * patients with known allergies to any of the study drugs, * patients with unstable hemodynamics, * patients who could not cooperate during postoperative pain assessment * patients who wanted to withdraw from the study, * patients with alcohol and drug addiction, * patients with musculoskeletal abnormalities

Design outcomes

Primary

MeasureTime frameDescription
Numeric Rating Scale (NRS) ScoresPostoperative 24 hoursDescription: 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.

Secondary

MeasureTime frameDescription
Dermatome AreaPostoperative 2 hours
Total tramadol consumptionPostoperative 24 hoursPostoperative total analgesic need was recorded as "milligram" in unit.

Countries

Turkey (Türkiye)

Contacts

CONTACTOĞUZ GÜNDOĞDU
droguzgundogdu@gmail.com+905545945469
CONTACTSAMET YENİHAN
samet_yenihan007@hotmail.com
PRINCIPAL_INVESTIGATOROĞUZ GÜNDOĞDU

Sivas Cumhuriyet University School of Medicine, Anesthesiology and Reanimation

STUDY_CHAIRSAMET YENİHAN

Sivas Cumhuriyet University School of Medicine, Anesthesiology and Reanimation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 4, 2026