Comparison of QIPB and SIFICB in Hip Surgery

NCT07233746 · tracked via the Priya Life Science Turkey tracker

Sponsor

Cumhuriyet University

Phase

Not applicable

Started

2025-12-15

Last updated

2025-11-18

Condition(s) studied

Postoperative PainHip Surgery

Investigational drug(s) / intervention(s)

Quadro-İliac Plane Block(QİPB)Suprainguinal Fascia Iliaca Compartiment Block

Quadro-İliac Plane Block(QİPB): 40 mL of 0.25% bupivacaine

Suprainguinal Fascia Iliaca Compartiment Block: 30 mL of 0.25% bupivacaine

Study summary

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

Sex

ALL

Min age

18 Years

Max age

99 Years

Healthy volunteers

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 abnormalitie

Primary outcome measure(s)

Numeric Rating Scale (NRS) Scores — Postoperative 24 hours
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.

Trial sites (1)

Facility	City	Region	Status
Sivas Cumhuriyet University School of Medicine, Anesthesiology and Reanimation	Sivas	Sivas

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07233746 on ClinicalTrials.gov ↗ ← All trials in Turkey