Actively Recruiting

Phase Not Applicable
Age: 18Years +
MALE
NCT06355076

New Urethral Reconstruction in Robot-assisted Laparoscopic Radical Resection

Led by Qilu Hospital of Shandong University · Updated on 2024-04-09

94

Participants Needed

1

Research Sites

173 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this clinical trial is to compare new reconstruction and anastomosis in robot-assisted radical laparoscopic resection It will also understand the possibility of exploring new reconstruction in completely solving patients' postoperative urinary incontinence The main questions it aims to answer are: Is there a significant improvement in urinary control in patients with new reconstruction compared with patients with anastomosis? The researchers compared the new reconstruction with anastomosis in robot-assisted laparoscopic radical resection to see if the new reconstruction improved urinary incontinence after operation. Participants will: The intervention group adopted the new reconstruction proposed by our team; End-to-end anastomosis was performed in non-intervention group.

CONDITIONS

Official Title

New Urethral Reconstruction in Robot-assisted Laparoscopic Radical Resection

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older with prostate cancer confirmed by biopsy
  • Tumor without extensive distant metastasis or in a resectable state after neoadjuvant chemotherapy and endocrine therapy
  • Willing to undergo robot-assisted laparoscopic radical prostatectomy
Not Eligible

You will not qualify if you...

  • Tumor metastasis not curable by surgery
  • Severe cardiovascular or cerebrovascular complications
  • Severe mental or neurological disorders
  • Poor liver or kidney function
  • Refusal to undergo robot-assisted laparoscopic radical prostatectomy

AI-Screening

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Trial Site Locations

Total: 1 location

1

Qilu hospital

Jinan, Shandong, China, 276600

Actively Recruiting

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Research Team

S

Shouzhen Chen, Dr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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