Skip to content

Prospective Study on the Safety and Feasibility of Single-Port Robot-Assisted Radical Prostatectomy Using a Stable Pneumoperitoneum System

Prospective Study on the Safety and Feasibility of Single-Port Robot-Assisted Radical Prostatectomy Using a Stable Pneumoperitoneum System

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117687
Enrollment
Unknown
Registered
2026-01-27
Start date
2025-08-04
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Prostate Cancer

Interventions

Single-Port Robot-Assisted Radical Prostatectomy Group:None
Multi-Port Robot-Assisted Radical Prostatectomy Group:None

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years old, male; 2.Preoperatively, the diagnosis of prostate adenocarcinoma was confirmed by pathology, and a radical prostatectomy was planned. 3.Before the operation, complete clinical data were available, including serum prostate-specific antigen (PSA), imaging data (such as MRI, ultrasound), and physical examination records, etc. 4.Participating in the preoperative and postoperative follow-up, and being able to accept the quality of life questionnaire and functional assessment; 5.Have the ability to sign the informed consent form and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1.Patients with a confirmed diagnosis of advanced or metastatic prostate cancer; 2.Patients who have previously received prostate cancer–related treatments (e.g., endocrine therapy, radiotherapy, surgery); 3.Patients with severe organ dysfunction, immune system diseases, or psychiatric disorders that contraindicate study participation; 4.Patients with incomplete data or unavailable imaging studies or biological samples; 5.Patients unwilling or unable to comply with study follow-up and data collection.

Design outcomes

Primary

MeasureTime frame
Intraoperative and postoperative complications;Postoperative Functional Recovery;Intraoperative blood loss;Duration of the surgery;

Secondary

MeasureTime frame
Intraoperative Pneumoperitoneum Stability;

Countries

China

Contacts

Public ContactQi Zhang

Zhejiang Provincial People's Hospital

clinic@126.com+86 138 5801 9285

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026