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Renal StonesNCT07360041

Comparison of ESWL and Mini-PCNL for High-Density Renal Stones in Children

A study testing Miniaturized Percutaneous Nephrolithotomy (mini-PNL) and Shock Wave Lithotripsy (SWL) in people with Renal Stones and Calculus, run by Ain Shams University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Pediatric nephrolithiasis is an increasing health problem, with rising prevalence particularly in certain geographic regions. Management options for pediatric renal stones include extracorporeal shockwave lithotripsy (SWL), percutaneous nephrolithotomy (PNL), and retrograde intrarenal surgery. Read more about this study

Who is it for?
Ages 2 to 12 years
Conditions the study is for
Renal Stones, Calculus, Pediatric
What is being tested?
Miniaturized Percutaneous Nephrolithotomy (mini-PNL) and Shock Wave Lithotripsy (SWL)
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteEgypt
Study dates
28 May 2023to 9 Sep 2025
Phase
Interventional
Are there results?
None posted in the registry

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 2 to 12 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Children from ages 2 to 12
  • Single renal stone pelvic, upper or middle calyceal
  • Stone diameter between 1 and 2 cm in the longest axis by NCCT
  • High-density (≥1000 HU) by NCCT

Who cannot join

  • Radiolucent stones
  • Co-existing renal anomalies
  • Acute UTI
  • Uncorrectable bleeding disorders
  • Musculoskeletal deformities
  • Patients with ureteral stones or ureteral obstruction

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Ain Shams University

    Cairo, Cairo Governorate, 4240112

Other trials in Egypt

About this study

Official title: Are Extracorporeal Shock Wave Lithotripsy and Mini-Percutaneous Nephrolithotomy Equivalent in The Management of Pediatric High-Density Renal Stones? A Prospective Randomized Study

Pediatric nephrolithiasis is an increasing health problem, with rising prevalence particularly in certain geographic regions. Management options for pediatric renal stones include extracorporeal shockwave lithotripsy (SWL), percutaneous nephrolithotomy (PNL), and retrograde intrarenal surgery. According to the EAU/ESPU guidelines, SWL is recommended as a first-line treatment for most renal stones; however, its success is significantly influenced by stone size, location, and density. High-density renal stones (≥1000 Hounsfield Units) are associated with lower stone-free rates after SWL and higher retreatment rates.

Miniaturized percutaneous nephrolithotomy (mini-PNL) has emerged as an effective alternative, offering high stone-free rates with reduced morbidity compared to standard PNL due to the use of smaller access sheaths. While adult studies have demonstrated superior outcomes of mini-PNL over SWL for high-density renal stones, there is a lack of comparative data in the pediatric population.

Read more

This prospective randomized controlled study aims to compare the efficacy and safety of mini-PNL versus SWL in children aged 2 to 12 years with single, non-lower pole, high-density (≥1000 HU), medium-sized (10-20 mm) renal stones. Eligible patients will be randomized into two equal groups to undergo either mini-PNL or SWL under general anesthesia.

The primary outcome is the stone-free rate, defined as no residual stone or residual fragments ≤4 mm on non-contrast computed tomography performed three months after the procedure. Secondary outcomes include operative and fluoroscopy times, hemoglobin drop, length of hospital stay, retreatment and ancillary procedure rates, and postoperative complications graded according to the Clavien-Dindo classification.

The study will be conducted at a single tertiary referral center. All participants' parents or legal guardians will provide informed consent in accordance with Good Clinical Practice guidelines and the Declaration of Helsinki. This study aims to provide evidence to guide optimal management of pediatric patients with high-density renal stones.

Read the detailed description

INTRODUCTION:

While nephrolithiasis is far more common in adults, pediatric stone disease is increasing in prevalence, especially in adolescent females , with higher incidences in the Middle East and North Africa and less common in North America and Europe . The management of pediatric upper urinary tract stones includes extracorporeal shockwave lithotripsy (SWL), percutaneous nephrolithotomy (PNL), and retrograde intrarenal surgery (RIRS).

SWL is a non-invasive procedure that can be performed in children. The European Association of Urology and European Society for Pediatric Urology (EAU/ESPU) guidelines recommend SWL as the primary treatment option for majority of renal stones and upper ureter stones. The stone-free rate (SFR) is significantly affected by various factors; stone location, size and density. Also, presence and degree of obstruction/impaction, and stone-to-skin distance affect SFR. SWL has SFR of nearly 90% for stones <1 cm, 80% for 1-2 cm, 60% for >2 cm. Concerns about anaesthesia and high retreatment rate represent SWL drawback .

The EAU/ESPU guidelines recommend PNL as a mainline of treatment in renal stones larger than 2 cm in the renal pelvis or more than 1 cm in lower pole stone as well as staghorn stones , as the SFR of PNL is between 86.9% and 98.5% after a single session, even in complete staghorn cases, it has a clearance rate of 89%. The PNL complications in children include bleeding, postoperative fever or infection, and persistent urinary leakage. With the miniaturised PNL (mini-PNL) through a 16-18F sheath, the transfusion rates and complications decreased.

The EAU/ESPU guidelines recommended SWL as a primary treatment for renal pelvis, 10-20 mm . However, some authors reported that SWL in children was more successful for stones with HU <1000.Also, in another recent study for adult patients with single, non-lower pole, high-density (≥1000 HU) renal stones, the SFR was 97.1% in the mini-PNL group versus 30.3% in the SWL group .

To the best of our knowledge, no studies in the pediatric population compared mini-PNL and SWL for single, non-lower pole, high-density (≥1000 HU) medium sized renal stones. In this study we will try to fill this gap in the literature

AIM OF THE STUDY:

To compare the outcomes of miniaturised percutaneous nephrolithotomy (mini-PNL) and extracorporeal shockwave lithotripsy (SWL) in the management of 10-20 mm, non-lower pole, high-density (≥1000 HU) renal stones in the pediatric population.

PATIENTS AND METHODS Primary outcome 1.Is to assess the efficacy using stone free rate defined as no or stone fragment residual ≤ 4 mm by non-contrast computed tomography (NCCT) 3 months after the procedure.

Secondary outcomes

1.To assess the operative time, fluoroscopy time, haemoglobin drop, hospital stay, retreatment rate, ancillary procedure and the complications using the Clavien-Dindo system as described at European Association of Urology Guidelines Panel in Reporting and grading of complications after urologic surgical procedures.

Study Design:

The design of the research will be a prospective randomised controlled study. Study Setting/Location The study will be conducted in a single tertiary centre at urology department at Ain Shams University Hospital, Egypt.

Parents of eligible children presented with renal stone will be asked to participate in this study and will be provided with an informed consent form in line with Good Clinical Practise and the Declaration of Helsinki.

I.Eligibility Criteria

Inclusion criteria are:

  1. Children from ages 2 to 12
  2. Single renal stone pelvic, upper or middle calyceal
  3. Stone diameter between 1 and 2 cm in the longest axis by NCCT
  4. High-density (≥1000 HU) by NCCT

The exclusion criteria are:

  1. Radiolucent stones
  2. Co-existing renal anomalies
  3. Acute UTI
  4. Uncorrectable bleeding disorders
  5. Musculoskeletal deformities
  6. Patients with ureteral stones or ureteral obstruction Enrollment of the participants All patients will be assessed preoperatively by detailed medical history, physical examination, urinalysis, urine culture, kidneys, ureters and bladder (KUB) x-ray, renal ultrasonography (US) and a NCCT, as well as a routine preoperative evaluation.

Randomization and allocation Eligible and consenting participants will be randomized in 2 equal groups to intervention mini-PNL or SWL group. Randomization will be produced with a computer-generated program in permuted blocks of random lengths Technique All procedures will be done under general anesthesia.

  1. Mini-PNL: All procedures will be done in the prone position. The target calyx will be punctured using fluoroscopic guidance with an 18-GA sheathed needle, and tract dilatation will be achieved using Amplatz dilators up to 16-18 Fr according to patient age. The holmium: YAG laser will be used to perform the stone fragmentation. Standard 12-Fr rigid nephroscope will be used for stone retrieval and fragmentation. A clamped nephrostomy tube will be placed routinely to reduce the bleeding for 24 h in all cases. The nephrostomy tube and the ureteral catheter will be removed on first and second postoperative days if there will be no complications.
  2. SWL: The lithotripsy will be performed by an electromagnetic shockwave lithotripter (Dornier Compact Sigma). The lung and genitourinary fields will be shielded for all patients. Fluoroscopy will be used to localize the stone and to monitor fragmentation. The dispensed shockwave will begin at 14 kV and escalates to its maximum power level of 20 kV. The maximum number of shocks given per session will be between 1000 and 2500 depending on patient age (1000 waves per session for children younger than 5 years and 2500 waves per session for older children, with a frequency of 70 shocks/minute). The SWL session will be stopped when no visible stone is detected, or when tiny fragments are the only visible stone remnants, or when the desired number of shocks has been given.

Follow up:

Patients will be assessed 2 weeks after the procedure by KUB and US to assess SFR. SWL will be repeated in cases with residual stone fragments > 4mm for a maximum of 3 sessions. NCCT will be performed at 3 month post the procedure to assess the final SFR.

The following data will be recorded: patient age, gender, BMI, patient's complaint, stone location and diameter, operative and fluoroscopy time, hemoglobin drop, postoperative complications, hospital stay, need for retreatment, auxiliary procedures, and stone free rate.

STATISTICAL CONSIDERATIONS AND DATA ANALYSIS Sample size and statistical power Using G* power programme and chi-square test to calculate sample size. During the study, the minimal accepted total sample size will be 40 based on effect size of 0.76 based on the previous trial published recently (12) with a 99 % power "beta", 0.05 level of significance is considered "alpha". The sample size will be increased to be 40 patients in each group due to expected dropout rate.

Statistical Analysis Continuous data will be summarized using the mean ± SD and compared by t test. Categorical variables will be compared using the χ2 test or Fisher's exact test. The Statistical Package for Social Sciences, version 13.0, for Windows (SPSS, Chicago, IL) will be applied for statistical analysis. P≤.05 will be considered statistically significant.

Compliance with ethical standards Conflict of interest: The authors declare that they have no conflict of interest.

Human and animal rights: All procedures in this study involving human participants were in accordance with the 1964 Helsinki Declaration and its later amendments.

Informed consent: Informed consent will be obtained from all individual participants in this study

Being tested
Miniaturized Percutaneous Nephrolithotomy (mini-PNL), Shock Wave Lithotripsy (SWL)
Keywords
10-20 mm non lower calyceal high density renal stones, renal, calculus, pediatrics, ESWL, PCNL
Medical subject headings
Nephrolithiasis, Calculi

What participants receive

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

  • Miniaturized Percutaneous Nephrolithotomy (mini-PNL)Procedure or surgery

    Mini-PNL: All procedures will be done in the prone position. The target calyx will be punctured using fluoroscopic guidance with an 18-GA sheathed needle, and tract dilatation will be achieved using Amplantz dilators up to 16-18 Fr according to patient age. The holmium: YAG laser will be used to perform the stone fragmentation. Standard 12-Fr rigid nephroscope will be used for stone retrieval and fragmentation. A clamped nephrostomy tube will be placed routinely to reduce the bleeding for 24 h in all cases. The nephrostomy tube and the ureteral catheter will be removed on first and second postoperative days if there will be no complications.

  • Shock Wave Lithotripsy (SWL)Procedure or surgery

    The lithotripsy will be performed by an electromagnetic shockwave lithotripter (Dornier Compact Sigma). The lung and genitourinary fields will be shielded for all patients. Fluoroscopy will be used to localize the stone and to monitor fragmentation.The dispensed shockwave will begin at 14 kV and escalates to its maximum power level of 20 kV. The maximum number of shocks given per session will be between 1000 and 2500 depending on patient age (1000 waves per session for children younger than 5 years and 2500 waves per session for older children, with a frequency of 70 shocks/minute). The SWL session will be stopped when no visible stone is detected, or when tiny fragments are the only visible stone remnants, or when the desired number of shocks has been given.

Study groups in NCT07360041
Study groupRoleWhat they receive
Miniaturized Percutaneous Nephrolithotomy (mini-PNL)Active comparatorMiniaturized Percutaneous Nephrolithotomy (mini-PNL)
Receives: Procedure: Miniaturized Percutaneous Nephrolithotomy (mini-PNL)
Shock Wave Lithotripsy (SWL)Active comparatorShock Wave Lithotripsy (SWL)
Receives: Procedure: Shock Wave Lithotripsy (SWL)

What is being measured

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

  1. Assess the efficacy assessed as stone free rate

    defined as no or stone fragment residual ≤ 4 mm by non-contrast computed tomography (NCCT)

    Measured: 3 months

Timeline

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

  1. First posted22 Jan 2026
  2. Study start28 May 2023
  3. Primary completion20 May 2025
  4. Study completion9 Sep 2025

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
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07360041
Sponsor's protocol ID
FMASUMD127/2023
Status last verified
Dec 2025
First submitted
14 Jan 2026
Last updated
22 Jan 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

A study testing Miniaturized Percutaneous Nephrolithotomy (mini-PNL) and Shock Wave Lithotripsy (SWL) in people with Renal Stones and Calculus, run by Ain Shams 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 6 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: finished, as of the sponsor's last update on 22 Jan 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assess the efficacy assessed as stone free rate (time frame: 3 months). 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 22 Jan 2026.

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