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Not yet recruitingNCT07172373Updated Sep 15, 2025

Safety and Effectiveness of Antegrade Flexible Ureteroscopy-Assisted Percutaneous Nephrolithotomy for Staghorn Calculi

An interventional study of antegrade flexible ureteroscopy-assisted PCNL and single PCNL in Urolithiasis and Renal Stones, sponsored by Tianjin Medical University Second Hospital. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-09-15.

Sponsored by Tianjin Medical University Second Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Mar 2026, 7 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
420
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Objective This study aims to evaluate the safety and efficacy of antegrade flexible ureteroscopy-assisted PCNL for the treatment of staghorn calculi, compared with standard PCNL.

Methods This prospective, multicenter, randomized controlled trial plans to enroll 420 patients with staghorn calculi, randomly assigned into two groups: the experimental group (antegrade flexible ureteroscopy-assisted PCNL, n=210) and the control group (standard PCNL, n=210). The primary endpoint is stone-free rate (defined as no residual fragment ≥2 mm on postoperative CT). Secondary endpoints include operative time, number of percutaneous tracts, rate of secondary procedures, hemoglobin decrease, postoperative complications (Clavien-Dindo classification), and length of hospital stay. All patients will undergo CT evaluation on postoperative day 2. Subgroup analysis will be performed according to the number of stone branches (≥5 vs \<5).

Read the detailed description

Background Renal calculi are among the most common diseases in urology. Current treatment options include extracorporeal shock wave lithotripsy (ESWL), flexible ureteroscopic lithotripsy, and percutaneous nephrolithotomy (PCNL). For renal stones ≥2 cm, PCNL is the recommended first-line treatment.

However, because of the large stone burden and the involvement of multiple calyces, it is often difficult to achieve complete clearance with a single PCNL session. Excessive angulation of the nephroscope may increase the risk of infundibular tears and bleeding, and stones located in parallel or narrow infundibula may be difficult to access, reducing the one-stage stone-free rate. To improve outcomes, several strategies have been adopted:

Multiple percutaneous tracts: Establishing additional tracts allows access to calyces unreachable from the primary tract and increases stone-free rates. However, this also increases the risks of bleeding, infection, and injury to the kidney or adjacent organs. In addition, expansion of the first tract may cause perirenal hematoma or morphological changes due to urine extravasation, making subsequent punctures more challenging. Multiple tracts also prolong postoperative recovery and increase hospitalization costs. Staged procedures: The first PCNL session removes stones in the renal pelvis and accessible calyces, while residual stones are addressed in a second-stage retrograde ureteroscopy. This reduces the risks compared with multiple tracts, but prolongs the treatment cycle and increases costs. Endoscopic combined intrarenal surgery (ECIRS) with modified patient positions: Positions such as the modified supine split-leg, lateral decubitus, or female-specific "Galdakao-modified supine Valdivia" allow simultaneous use of ureteroscopic and percutaneous approaches. This combines the efficiency of PCNL with the wide access angle of ureteroscopy, reduces the need for repositioning under anesthesia, and facilitates intraoperative monitoring. However, it requires two surgical teams, duplicate equipment, and high coordination, which may prolong operative time.

Previous studies suggest that combining single-tract PCNL with flexible ureteroscopy and holmium laser lithotripsy may be an ideal approach for staghorn stones. While antegrade cystoscopic lithotripsy accommodates thicker fibers and offers faster irrigation and clearer visualization, the larger diameter of the cystoscope limits its passage through the ureter, risking residual fragments. Recently, antegrade flexible ureteroscopy-assisted PCNL has been attempted, but most studies are small retrospective series or case reports. The limited adoption may be due to the high purchase and repair costs of reusable flexible ureteroscopes. The development of single-use ureteroscopes has largely overcome these barriers, providing a foundation for multicenter prospective studies.

Based on this background, a multicenter clinical study of antegrade flexible ureteroscopy-assisted PCNL for staghorn calculi has important clinical value. Our preliminary work showed that when the number of stone branches was ≥5, the need for multiple tracts and staged procedures increased, while operative time was prolonged, hospital stay was longer, and the stone-free rate was reduced. We therefore further compared the efficacy of standard PCNL and antegrade flexible ureteroscopy-assisted PCNL stratified by stone branch number.

Objective To evaluate the safety and efficacy of antegrade flexible ureteroscopy-assisted PCNL in the treatment of staghorn calculi, compared with standard PCNL.

Study Overview Design This is a prospective, multicenter clinical study. Population

Inclusion criteria:

Diagnosis of staghorn calculi confirmed by non-contrast CT. Age ≥18 years. General condition suitable for surgery. Ability to understand and voluntarily sign informed consent.

Exclusion criteria:

Solitary kidney or congenital anomalies (e.g., horseshoe kidney, ectopic kidney). Severe preoperative pyelonephritis. Psychiatric illness or lack of cooperation. Uncontrolled comorbidities (e.g., diabetes, hypertension) contraindicating surgery. Coagulation disorders. Investigator's judgment of unsuitability.

Withdrawal criteria:

Subject withdrawal: refusal to continue or loss to follow-up. Investigator withdrawal: complications making continuation unsafe, or poor compliance.

Sample size and grouping

A total of 420 patients will be enrolled across 14 centers (30 per center). Patients will be randomized into two groups:

Experimental group: antegrade flexible ureteroscopy-assisted PCNL (n=210). Control group: standard PCNL (n=210).

Procedures All patients will undergo preoperative urine culture. Infected patients will receive targeted antibiotics until negative. Surgery will be performed under general anesthesia with tracheal intubation.

Standard PCNL group: Residual stones inaccessible through the primary tract will be managed by establishing a second or third tract.

Antegrade flexible ureteroscopy-assisted PCNL group: Residual stones will first be managed using a flexible ureteroscope introduced via the established tract. The Tianjin Institute of Urology (TJIU) technique will be adopted, systematically inspecting all calyces and the ureter. Additional tracts will be created only if necessary.

At the end of surgery, a double-J stent and nephrostomy tube will be placed. Postoperative evaluation: Stone-free rate (no residual fragments ≥2 mm on CT on postoperative day 2). Operative time (from tract establishment to nephrostomy placement). Complications (Clavien-Dindo classification). Secondary procedures. Postoperative fever. Length of hospital stay. Subgroup analysis will be conducted based on the number of stone branches (≥5 vs \<5).

Endpoints Primary endpoint: Stone-free rate. Secondary endpoints: surgeon-perceived smoothness of operation, treatment satisfaction, rate of secondary procedures, operative time, number of tracts, hemoglobin decrease, length of hospital stay, postoperative complications.

Adverse Events

Definitions:

Adverse event (AE): any unfavorable medical occurrence after treatment, not necessarily causally related.

Serious adverse event (SAE): hospitalization, prolonged hospitalization, disability, life-threatening condition, death, or congenital anomaly.

Severity:

Mild: tolerable, no specific treatment needed. Moderate: requires intervention, directly affects recovery. Severe: life-threatening, fatal, or disabling, requiring emergency treatment.

Reporting:

All AEs/SAEs will be documented in case report forms with onset, presentation, management, and outcome. SAEs will be reported within 24 hours to the sponsor, ethics committee, and regulatory authorities.

Statistical Analysis This randomized, open-label, multicenter trial uses stone-free rate (CT on day 2, no fragments ≥2 mm) as the primary outcome. Based on preliminary data (stone-free rate \~52% for PCNL and \~71% for antegrade flexible ureteroscopy-assisted PCNL), sample size was calculated with 90% power and α=0.025, requiring 157 patients per group. Allowing for 20% attrition, 210 patients per group (420 total) will be enrolled.

Data will be analyzed using R software (version 4.1.2). Continuous variables will be expressed as mean ± SD, categorical variables as frequencies and percentages. Student's t-test, chi-square test, or Fisher's exact test will be used as appropriate. Two-sided p-values \<0.05 will be considered statistically significant.

02

Conditions studied

  • Urolithiasis
  • Renal Stones

Keywords

  • Percutaneous nephrolithotomy
  • Antegrade flexible ureteroscopy
  • Staghorn calculi
  • Stone branch number
03

In context

Urolithiasis

253 studies on the registry are indexed under Urolithiasis; 67 are open to participants now.

This study's planned enrollment of 420 is above the median of 100 across 182 interventional studies indexed under Urolithiasis.

Browse Urolithiasis studies →

Lead sponsor

Tianjin Medical University Second Hospital is the lead sponsor of 60 studies on the registry; 36 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
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

Staghorn calculi confirmed by non-contrast CT of the urinary system; Age ≥18 years; General condition suitable for surgical treatment; Ability to understand and voluntarily sign the form.

Exclusion criteria

Exclusion Criteria:

Solitary kidney or congenital anomalies (such as horseshoe kidney or ectopic kidney); Patients with severe preoperative pyelonephritis; Patients with psychiatric disorders or unwilling to cooperate; Patients with uncontrolled diabetes or hypertension who cannot tolerate surgery; Patients with coagulation disorders; Patients deemed unsuitable for participation in this trial by the investigator.

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Care provider, Investigator, Outcomes assessor)
Enrollment
420 participants (estimated)

Study arms

  • Experimental
    antegrade flexible ureteroscopy-assisted PCNL

    antegrade flexible ureteroscopy-assisted PCNL

    Procedure: antegrade flexible ureteroscopy-assisted PCNL

  • Other
    single PCNL

    single PCNL

    Procedure: single PCNL

Interventions

  • Procedureantegrade flexible ureteroscopy-assisted PCNL

    antegrade flexible ureteroscopy-assisted PCNL

  • Proceduresingle PCNL

    single PCNL

06

What researchers measure

Primary outcomes

  1. Immediately stone-free rate (SFR)

    defined as no residual fragment ≥2 mm on postoperative CT

    Time frame: On postoperative day 2, a non-contrast CT of the urinary system will be performed, and the absence of residual fragments larger than 2 mm will be defined as stone-free.

Secondary outcomes

  1. Operative time

    Operative time

    Time frame: From the establishment of the first percutaneous renal tract to the placement of the final nephrostomy tube.

  2. Duration of hospital stay

    Duration of hospital stay

    Time frame: Up to 3 months.

  3. Complications

    Complications

    Time frame: Up to 3 months.

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — Individual participant data will not share to other researchers as ethical issues.

No publications or documents are linked to this record.

09

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

Start is estimated for Oct 2025; primary completion for Mar 2026, 5 months later.

Of 86 non-industry interventional studies with no phase under Urolithiasis, half reached primary completion within 20 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 40. This study's planned 5 months is below that.

Counting every sponsor, half of 96 studies reached it within 19 months; a quarter within 11 and three quarters within 39.

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

Registered
Sep 8, 2025
First posted
Sep 15, 2025
StartEst.
Oct 1, 2025
Primary completionEst.
Mar 30, 2026
CompletionEst.
Apr 30, 2026
Last update
Sep 15, 2025
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 Sep 15, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07172373
Lead sponsor
Tianjin Medical University Second Hospital
Collaborators
Chinese PLA General Hospital, Tianjin Medical University General Hospital, Peking University People's Hospital, First Hospital of China Medical University, The Second Affiliated Hospital of Dalian Medical University, The First Affiliated Hospital of Guangzhou Medical University, Second Affiliated Hospital of Guangzhou Medical University, The First Affiliated Hospital with Nanjing Medical University, Beijing Tsinghua Changgeng Hospital, The First Affiliated Hospital of Soochow University, Second Affiliated Hospital, School of Medicine, Zhejiang University, The Affiliated Hospital of Qingdao University, Wuhan TongJi Hospital
Responsible party
Sponsor
First posted
Sep 15, 2025
Start date
Oct 1, 2025 (estimated)
Primary completion
Mar 30, 2026 (estimated)
Completion
Apr 30, 2026 (estimated)
Last update
Sep 15, 2025

Study contacts

Yuanjiong Qi
Contact
qiyuanjiong@163.com
022-88328695

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

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