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Study on the Application of Single-Position Percutaneous Nephrolithotomy in the treatment of Urolithiasis

Study on the Application of Single-Position Percutaneous Nephrolithotomy in the treatment of Urolithiasis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101588
Enrollment
Unknown
Registered
2025-04-27
Start date
2024-04-11
Completion date
Unknown
Last updated
2025-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary calculus

Interventions

Single-position group:The patient undergoes surgery in a single-position.
Traditional prone position group:The patient undergoes surgery in the traditional prone position.

Sponsors

The Second Hospital of Tianjin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Signing a written informed consent form before enrollment. 2.Age >= 18 years, both males and females are eligible. 3.1) Renal pelvis or calyces single or multiple stones >= 2cm or stag horn stones 2) Patients requiring surgical treatment and have failed extracorporeal shock wave lithotripsy (ESWL) or retrograde intrarenal surgery (RIRS) for kidney stones 3) Combined with moderate to severe hydronephrosis, stones in the upper segment of the ureter with a diameter>=1.5cm, or stones in the renal pelvis-ureter junction Meeting at least one of the above conditions, and diagnosed by CT imaging; 4)Subjects voluntarily join this study, have good compliance, and cooperate with safety and survival follow-up

Exclusion criteria

Exclusion criteria: 1.Preoperative coagulation disorders or uncorrected systemic bleeding disorders. 2.Any severe cardiovascular or respiratory diseases. 3.Congenital renal abnormalities (such as horseshoe kidney, pelvic kidney, UPJO, etc.). 4.Use of anticoagulant or antiplatelet medications without discontinuation. 5.High risk of thrombotic events. 6.Patients unable to tolerate prone position surgery. 7.Subjects who have not signed the informed consent form. 8.Any other patients not suitable for entry into this study. 9.Patients planning for two-stage surgery preoperatively. 10.Pregnant patients.

Design outcomes

Primary

MeasureTime frame
Operation time;Stone free rates;

Secondary

MeasureTime frame
Postoperative complications;Incidence of postoperative SIRS;Hospitalization expenses;

Countries

China

Contacts

Public ContactChunyu Liu

The Second Hospital of Tianjin Medical University

prof_liucy@163.com+86 138 2198 5158

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026