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RecruitingNCT07523074Updated Apr 13, 2026

Early vs Delayed Extracorporeal Shock Wave Lithotripsy for Residual Stones After Percutaneous Nephrolithotomy

An interventional study of Extracorporeal shock wave lithotripsy (ESWL) in Nephrolithiasis, sponsored by Beni-Suef University. Recruiting at 1 site in Egypt. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-04-13.

Sponsored by Beni-Suef University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Dec 2025, registered Apr 2026).
  • Started Dec 2025; still recruiting 11 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
476
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
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Study summary

Residual renal stone fragments remain a common clinical issue following percutaneous nephrolithotomy (PCNL), with reported incidence ranging from 10% to 30%. These fragments may act as a nidus for recurrent stone formation, infection, or obstruction, necessitating further intervention. Extracorporeal shock wave lithotripsy (ESWL) is widely used as a non-invasive treatment option for such residual stones; however, the optimal timing of ESWL after PCNL remains unclear.

Early application of ESWL may enhance stone clearance before fragment embedding or encrustation occurs, but it could be associated with increased risk of bleeding or infection due to incomplete renal healing. Conversely, delayed ESWL allows for better tissue recovery but may permit stone growth or persistence of symptoms.

This prospective randomized comparative study aims to evaluate the optimal timing of ESWL after PCNL in patients with residual renal stones ≤15 mm. Eligible patients will be randomized into two groups: early ESWL (within 7-14 days after PCNL) and delayed ESWL (after 3-4 weeks). The primary outcome is the stone-free rate at 3 months, while secondary outcomes include complication rates, pain scores, renal function changes, and the need for additional interventions.

The results of this study are expected to provide evidence-based guidance on the ideal timing of ESWL following PCNL to maximize efficacy and minimize complications.

Read the detailed description

Percutaneous nephrolithotomy (PCNL) is considered the gold standard treatment for large and complex renal stones. Despite advances in surgical techniques and imaging, residual stone fragments (RFs) remain a relatively common finding after PCNL, with reported rates ranging from 10% to 30%. These residual fragments are clinically significant, as they may serve as a nidus for recurrent stone formation, urinary tract infection, obstruction, and the need for secondary interventions.

Extracorporeal shock wave lithotripsy (ESWL) is a widely accepted, non-invasive modality for the management of residual renal stones following PCNL. However, the optimal timing for performing ESWL after PCNL remains controversial. Early ESWL may improve stone clearance rates by targeting fragments before they become embedded within the collecting system or undergo encrustation. On the other hand, early intervention may be associated with an increased risk of complications, such as bleeding or infection, due to incomplete renal parenchymal healing after PCNL.

Delayed ESWL allows for adequate healing of renal tissue, potentially reducing procedure-related complications. However, postponing treatment may allow residual fragments to increase in size, migrate, or become symptomatic, which could negatively impact overall outcomes and increase the likelihood of additional interventions.

Given this clinical uncertainty, this study is designed as a prospective, randomized, comparative clinical trial to evaluate the optimal timing of ESWL after PCNL. Patients who undergo PCNL and are found to have residual renal stones measuring ≤15 mm on postoperative imaging (non-contrast CT or ultrasound) will be considered eligible for inclusion.

Eligible participants will be randomly assigned in a 1:1 ratio into two groups:

Group A (Early ESWL): Patients will undergo ESWL within 7-14 days after PCNL. Group B (Delayed ESWL): Patients will undergo ESWL after 3-4 weeks following PCNL.

All patients will be treated using the same lithotripter system, with standardized ESWL parameters (energy level, frequency, and number of shocks) according to current European Association of Urology (EAU) guidelines. A maximum of three ESWL sessions will be allowed per patient, with appropriate analgesia or sedation provided as needed.

Patients will be followed up clinically and radiologically. Imaging (ultrasound or non-contrast CT) will be performed after completion of ESWL sessions to assess stone clearance. Stone-free status will be defined as the absence of residual fragments greater than 2 mm. Final assessment of the primary outcome will be conducted at 3 months.

The primary outcome measure of the study is the stone-free rate (SFR) at 3 months.

Secondary outcome measures include:

Procedure-related complications (e.g., hematuria, fever, urinary tract infection, steinstrasse) Post-procedural pain assessed using the visual analog scale (VAS) Changes in renal function (serum creatinine) Need for auxiliary procedures such as ureteroscopy (URS) or repeat PCNL Statistical analysis will be performed using SPSS software. Continuous variables will be expressed as mean ± standard deviation and compared using Student's t-test. Categorical variables will be expressed as percentages and compared using the Chi-square test. A p-value \< 0.05 will be considered statistically significant. Analysis will be conducted on an intention-to-treat basis.

This study aims to provide high-quality evidence regarding the optimal timing of ESWL after PCNL, which may help improve clinical outcomes, reduce complications, and guide future urological practice guidelines.

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Conditions studied

  • Nephrolithiasis

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03

In context

Nephrolithiasis

324 studies on the registry are indexed under Nephrolithiasis; 90 are open to participants now.

This study's planned enrollment of 476 is above the median of 92 across 257 interventional studies indexed under Nephrolithiasis.

Browse Nephrolithiasis studies →

Lead sponsor

Beni-Suef University is the lead sponsor of 349 studies on the registry; 125 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18-70 years.
  • Single or multiple residual renal stones ≤15 mm after PCNL.
  • Normal renal function (serum creatinine \<1.5 mg/dL).
  • No active UTI.

Exclusion criteria

Exclusion Criteria:

  • Bleeding disorders or anticoagulant therapy.
  • Obstructed drainage or active sepsis.
  • Stones >15 mm or requiring secondary PCNL.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
476 participants (estimated)

Study arms

  • Experimental
    (Early ESWL): ESWL within 7-14 days after PCNL

    Patients receive extracorporeal shock wave lithotripsy (ESWL) within 7-14 days after percutaneous nephrolithotomy (PCNL) for treatment of residual renal stones ≤15 mm. Standard ESWL protocol is applied with a maximum of 3 sessions.

    Procedure: Extracorporeal shock wave lithotripsy (ESWL)

  • Experimental
    (Delayed ESWL): ESWL after 3-4 weeks.

    Patients receive extracorporeal shock wave lithotripsy (ESWL) 3-4 weeks after percutaneous nephrolithotomy (PCNL) for treatment of residual renal stones ≤15 mm. Standard ESWL protocol is applied with a maximum of 3 sessions.

    Procedure: Extracorporeal shock wave lithotripsy (ESWL)

Interventions

  • ProcedureExtracorporeal shock wave lithotripsy (ESWL)

    Extracorporeal shock wave lithotripsy (ESWL) is performed using a standardized protocol for treatment of residual renal stones ≤15 mm after percutaneous nephrolithotomy (PCNL). All patients are treated using the same lithotripter model with standardized energy settings and shock frequency according to EAU guidelines. Sedation is administered as needed. A maximum of three ESWL sessions is allowed. Follow-up imaging is performed to assess stone clearance.

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What researchers measure

Primary outcomes

  1. Stone-Free Rate at 3 Months

    The proportion of patients who are stone-free, defined as no residual fragments greater than 2 mm on imaging (ultrasound or CT scan) at 3 months after ESWL treatment.

    Time frame: 3 months after ESWL

Secondary outcomes

  1. Complication Rate

    The incidence of postoperative complications including hematuria, fever, and urinary tract infection following ESWL treatment.

    Time frame: Within 4 weeks after ESWL

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Study locations

1 of 1 sites recruiting
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References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: Undecided

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Dec 2025 (actual). Primary completion is estimated for Oct 2026, 10 months after the start.

Of 134 non-industry interventional studies with no phase under Nephrolithiasis, half reached primary completion within 25 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 40. This study's planned 10 months is below that.

Counting every sponsor, half of 140 studies reached it within 24 months; a quarter within 12 and three quarters within 38.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 5, 2026
First posted
Apr 13, 2026
StartActual
Dec 2, 2025
Primary completionEst.
Oct 2026
CompletionEst.
Dec 2026
Last update
Apr 13, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07523074
Responsible party
Mahmoud Abdallah (lecturer of urology Beni-Suef university hospital, Beni-Suef University) — Principal investigator
First posted
Apr 13, 2026
Start date
Dec 2, 2025
Primary completion
Oct 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Apr 13, 2026

Study contacts

Mahmoud Abdallah Mahmoud, lecturer of urology
Contact
mahmoud.abdalla@med.bsu.edu.eg
+2001155361979

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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