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Recruiting Not applicable

Safety and Efficacy of Papillary Versus NonPapillary Access During Percutaneous Nephrolithotomy

NCT07855354 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-11-01
Last updated
2026-10-02

Condition(s) studied

SafetyEfficacyPapillaryNonPapillaryPercutaneous Nephrolithotomy

Investigational drug(s) / intervention(s)

Papillary access punctureNon-papillary access puncture

Papillary access puncture: Patients will undergo papillary access puncture (Control group)

Non-papillary access puncture: Patients will undergo non-papillary access puncture

Study summary

This study aims to evaluate and compare the safety, efficacy, and clinical outcomes of papillary and non-papillary renal access during percutaneous nephrolithotomy (PCNL), and to determine whether non-papillary puncture can be considered a safe and effective alternative to the conventional papillary approach in selected patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years * Solitary or multiple renal calculi ≥2 cm * Ability to provide informed consent Exclusion Criteria: * Bleeding diathesis or uncorrected coagulopathy * Active urinary tract infection at the time of surgery * Congenital anomalies severely distorting renal anatomy (e.g., horseshoe kidney, ectopic kidney) * Morbid obesity \[body mass index (BMI) ≥ 40\] limiting safe positioning * Pregnancy

Primary outcome measure(s)

  • Stone-free rate — 4 weeks postoperatively
    Stone-free rate will be assessed at 4 weeks postoperatively using non-contrast computed tomography (CT). It will be defined as the absence of residual stones or the presence of clinically insignificant residual fragments (asymptomatic, non-obstructive fragments 2:3mm).

Trial sites (1)

FacilityCityRegionStatus
Ain Shams University Cairo Egypt Recruiting
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 NCT07855354 on ClinicalTrials.gov ↗ ← All trials in Egypt