Skip to content

A clinical trial of urological surgery with a single-hole endoscopic system

A clinical trial of urological surgery with a single-hole endoscopic system

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085544
Enrollment
Unknown
Registered
2024-06-12
Start date
2023-09-18
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Stenosis of ureter

Interventions

experimental group:Shurui endoscopic single-hole surgery system

Sponsors

Beijing Miyun District Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (pyeloplasty) Pyeloplasty is required for UPJO patients; Age 18-75 years old, gender unlimited; Agree to sign informed consent forms and be able to follow medical advice and regular follow-up visits. (Excision of adrenal tumor) Patients requiring adrenal tumor resection to treat adrenal masses; Adenoma less than 4cm Age 18-75 years old, gender unlimited; Agree to sign informed consent forms and be able to follow medical advice and regular follow-up visits. (partial nephrectomy) Eligible patients requiring partial nephrectomy; Age 18-75 years old, gender unlimited; Agree to sign informed consent forms and be able to follow medical advice and regular follow-up visits. (Radical resection of prostate cancer) Prostate cancer patients requiring radical prostate cancer surgery; Men aged 18-75; Agree to sign informed consent forms and be able to follow medical advice and regular follow-up visits.

Exclusion criteria

Exclusion criteria: Does not meet the inclusion criteria; There are serious uncontrolled diseases and acute infections; Patients with cardiovascular and cerebrovascular diseases, blood system diseases and diabetes, and their control conditions cannot meet surgical standards; Patients with immune system diseases whose control conditions cannot meet surgical standards; Patients with intellectual problems and mental disorders; Patients with a history of abdominal and pelvic surgery and severe abdominal and pelvic adhesions;

Design outcomes

Primary

MeasureTime frame
Operation success rate;

Secondary

MeasureTime frame
Surgical margin;Postoperative urinary incontinence;Postoperative urinary tract obstruction;intraoperative blood loss;Prostate Specific Antigen;Warm ischemic time;operative time;

Countries

China

Contacts

Public ContactYaming Gu

Beijing Miyun District Hospital

gymmiyun@126.com+86 136 6134 2987

Outcome results

None listed

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