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NephrolithiasisNCT07523074

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

A study testing Extracorporeal shock wave lithotripsy (ESWL) in people with Nephrolithiasis, run by Beni-Suef University at 1 site in Egypt.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Nephrolithiasis
What is being tested?
Extracorporeal shock wave lithotripsy (ESWL)
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
476 participants
Where
1 siteEgypt
Study dates
2 Dec 2025to Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Mahmoud Abdallah Mahmoud, lecturer of urology contact

+2001155361979

mahmoud.abdalla@med.bsu.edu.eg

Egypt1 site, 1 recruiting
  • Beni-Suef university hospital

    Banī Suwayf, Beni-Suef Governrate, 62511

    Doaa Mohamed Khalil, Lecturer, +0201152091011, drm_abdallah_88@yahoo.com

    Recruiting

Other trials in Egypt

About this study

Official title: Optimum Time for Extracorporeal Shock Wave Lithotripsy for Residual Stones After Percutaneous Nephrolithotomy: A Prospective Comparative Randomized Study

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.

Read more

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.

Conditions
Nephrolithiasis
Being tested
Extracorporeal shock wave lithotripsy (ESWL)
Medical subject headings
Nephrolithiasis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Extracorporeal shock wave lithotripsy (ESWL)Procedure or surgery

    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.

Study groups in NCT07523074
Study groupRoleWhat they receive
(Early ESWL): ESWL within 7-14 days after PCNLExperimentalPatients 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.
Receives: Procedure: Extracorporeal shock wave lithotripsy (ESWL)
(Delayed ESWL): ESWL after 3-4 weeks.ExperimentalPatients 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.
Receives: Procedure: Extracorporeal shock wave lithotripsy (ESWL)

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: 3 months after ESWL

Secondary outcomes (1)
  1. Complication Rate

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

    Measured: Within 4 weeks after ESWL

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Apr 2026
  2. Study start2 Dec 2025
  3. Primary completionOct 2026 (estimated)
  4. Study completionDec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
476 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07523074
Sponsor's protocol ID
FMBSUREC/02122025/Abdallah
Status last verified
Apr 2026
First submitted
5 Apr 2026
Last updated
13 Apr 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Extracorporeal shock wave lithotripsy (ESWL) in people with Nephrolithiasis, run by Beni-Suef University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 13 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Mahmoud Abdallah Mahmoud, lecturer of urology (+2001155361979, mahmoud.abdalla@med.bsu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Stone-Free Rate at 3 Months (time frame: 3 months after ESWL). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Apr 2026.

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