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Clinical Trials in China / NCT07408050
Enrolling by invitation Not applicable

An Investigation Into the Application of Preputial Grafts for the Reconstruction of Complex Ureteral Strictures

NCT07408050 · tracked via the Priya Life Science China tracker
Sponsor
Ruibao chen
Phase
Not applicable
Started
2026-08-03
Last updated
2026-08-04

Condition(s) studied

Ureteral Stenosis

Investigational drug(s) / intervention(s)

Preputial graft ureteroplasty

Preputial graft ureteroplasty: Reconstruction of complex ureteral stenosis using preputial graft

Study summary

Complex ureteral stricture refers to a ureteral lumen stenosis lesion that cannot be directly treated with the traditional end-to-end anastomosis. In recent years, its incidence has shown a gradual upward trend, and it has long been a major clinical challenge for urological surgeons. Because it is difficult to achieve tension-free anastomosis after direct resection of the strictured segment, which can easily lead to the failure of stricture repair surgery, simple ureteral stricture segment resection combined with end-to-end anastomosis is generally not recommended for the treatment of such diseases.

In general, clinicians need to select alternative materials for ureteral reconstruction, such as Boari flap, appendix, intestinal tract, and oral mucosa, to achieve the surgical effect of tension-free anastomosis. However, in some complex clinical cases, if Boari flap, appendix, intestinal tract or oral mucosa cannot be used for surgery, or if patients refuse to accept oral mucosa, intestinal mucosa and other tissues for ureteral repair, are there any other alternative schemes with high safety and minimal invasiveness available for ureteral reconstruction in clinical practice? Thus, it is of great clinical significance to develop safe, effective and innovative surgical techniques for ureteral reconstruction. Circumcision is a surgical procedure with a long history and wide application, and the prepuce removed during the operation is usually treated as medical waste. Our research team has previously performed a large number of surgeries using prepuce to repair the urethra. Clinical results have shown that free prepuce has the advantages of easy survival, convenient harvesting and minimal invasiveness, making it an ideal graft material for urinary tract repair and reconstruction.

At present, there have been case reports on ureteral reconstruction using prepuce abroad. Based on our team's previous research experience in the fields of urethral reconstruction and ureteral reconstruction, the investigators intend to carry out relevant research on ureteral reconstruction with free preputial grafts, aiming to obtain convincing clinical data and provide a more minimally invasive and safer new treatment option for the repair and reconstruction of complex ureteral strictures.

Eligibility

Sex
MALE
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria * Male patients over 18 years of age. * Preoperative assessment confirming complex ureteral strictures, characterized by ureteral luminal stenosis that cannot be addressed via conventional end-to-end anastomosis. Patients were deemed ineligible for existing surgical. interventions such as pyeloureteroplasty, ureteral end-to-end anastomosis, and ureteroneocystostomy. * Ability to undergo minimally invasive laparoscopic surgery for ureteral stricture repair. * Presence of redundant prepuce or availability of an inner preputial flap for graft harvesting. * Capacity for independent decision-making and willingness to voluntarily sign the informed consent form for study participation. Exclusion Criteria * Presence of surgical contraindications. * History of abdominal radiotherapy. * Ureteral strictures resulting from malignant tumors. * An Eastern Cooperative Oncology Group (ECOG) performance status score greater than 2. * Poor compliance or other exclusion criteria as determined by the investigators.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan Hubei
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07408050 on ClinicalTrials.gov ↗ ← All trials in China