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.
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.
Egypt1 site, 1 recruiting
- Recruiting
Beni-Suef university hospital
Banī Suwayf, Beni-Suef Governrate, 62511
Doaa Mohamed Khalil, Lecturer, +0201152091011, drm_abdallah_88@yahoo.com
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 group | Role | What they receive |
|---|---|---|
| (Early ESWL): ESWL within 7-14 days after PCNL | Experimental | 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. Receives: Procedure: Extracorporeal shock wave lithotripsy (ESWL) |
| (Delayed ESWL): ESWL after 3-4 weeks. | Experimental | 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. Receives: Procedure: Extracorporeal shock wave lithotripsy (ESWL) |
What is being measured
The primary outcome is the main question the study is designed to answer.
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)
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.
- First posted13 Apr 2026
- Study start2 Dec 2025
- Primary completionOct 2026 (estimated)
- Study completionDec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for NephrolithiasisStudies of the same condition, open and under way.
- More trials run by Beni-Suef UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Beni-Suef University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mahmoud Abdallah, Beni-Suef University
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
Study at a glance
From the registry record, last updated by the sponsor on 13 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Optimum Time for Extracorporeal Shock Wave Lithotripsy for Residual Stones After Percutaneous Nephrolithotomy: A Prospective Comparative Randomized Study
- ClinicalTrials.gov ID
- NCT07523074
- Acronym / sponsor ID
- FMBSUREC/02122025/Abdallah
- Conditions
- Nephrolithiasis
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 476 participants (estimated)
- Lead sponsor
- Beni-Suef UniversityUniversity, hospital or other
- Study start
- 2 Dec 2025 (actual)
- Primary completion
- Oct 2026 (estimated)
- Study completion
- Dec 2026 (estimated)
- First posted
- 13 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| (Early ESWL): ESWL within 7-14 days after PCNL | Experimental | Procedure: Extracorporeal shock wave lithotripsy (ESWL)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. |
| (Delayed ESWL): ESWL after 3-4 weeks. | Experimental | Procedure: Extracorporeal shock wave lithotripsy (ESWL)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. |
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- 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.
Key exclusion criteria (3 listed)
- Bleeding disorders or anticoagulant therapy.
- Obstructed drainage or active sepsis.
- Stones >15 mm or requiring secondary PCNL.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Extracorporeal 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. | Procedure or surgery | (Delayed ESWL): ESWL after 3-4 weeks., (Early ESWL): ESWL within 7-14 days after PCNL |
Primary outcome
Stone-Free Rate at 3 Months
Time frame: 3 months after ESWL
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.
1 secondary outcome
Complication Rate
Time frame: Within 4 weeks after ESWL
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Apr 2026.
- Individual participant dataSharing planned: Undecided
Related trials for Nephrolithiasis
Not yet recruiting
Automated Versus Manual Irrigation During Flexible Ureteroscopy
Renal Stone Disease
Not yet recruiting
Optimal Intrarenal Pressure During Flexible Ureteroscopy
Renal Stone Disease
RecruitingObservational study
Stone Clearance With Aspiration vs Other Technologies: a Real-world Evidence Study
Urolithiasis, Stones, Kidney
Not yet recruiting
Intertransverse Process Block Versus Erector Spinae Plane Block for Postoperative Analgesia After Percutaneous Nephrolithotomy
Kidney Stones, Urolithiasis, Hypocitraturia, Pain, Postoperative
Not yet recruiting
Comparison of Smart Pressure-Controlled Flexible Ureteroscopy and Flexible Suction Ureteral Access Sheath-Assisted Flexible Ureteroscopy for 2-3 cm Renal Stones
Kidney Stones
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
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.