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A prospective, non randomized, concurrent controlled study on the feasibility and safety of removing urinary catheters 5 days after laparoscopic radical prostatectomy

A prospective, non randomized, concurrent controlled study on the feasibility and safety of removing urinary catheters 5 days after laparoscopic radical prostatectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075295
Enrollment
Unknown
Registered
2023-08-31
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

prostate cancer

Interventions

experimental group:Urinary catheter removal 5 days after laparoscopic radical prostatectomy
control group:Urinary catheter removal 14 days after laparoscopic radical prostatectomy

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age: 50-75 years old 2. T1-3NxM0 prostate cancer patients who undergo laparoscopic radical prostatectomy, T1-3NxM0 prostate cancer patients have received neoadjuvant endocrine therapy for no more than 3 months before surgery can be included; 3. Be able to cooperate and complete follow-up and related examinations; 4. Agree to participate in this experiment and sign an informed consent form

Exclusion criteria

Exclusion criteria: 1. Preoperative complications such as urethral stricture, neurogenic bladder, cognitive impairment, and other malignant tumors were not cured; 2. Previous medical history of receiving prostate cancer treatment, including surgery, long-term endocrine therapy (over 3 months), chemotherapy, radiotherapy, targeted therapy, and immunotherapy; 3. Have a history of pelvic and lower abdominal surgeries; Patients with a history of prostate resection/enucleation surgery; 4. Concurrent with serious other systemic diseases, according to the judgment of the researcher, may interfere with the treatment, evaluation, or compliance of the trial; 5. Contraindications to radical prostatectomy for prostate cancer 6. Participate in any other ongoing experiments.

Design outcomes

Primary

MeasureTime frame
Complete urinary continence rate at 3 months after surgery;Complete urinary continence rate at 12 months after surgery;Incidence rate of urinary fistula within 3 months after operation;Incidence rate of urinary retention within 3 months after operation;

Secondary

MeasureTime frame
The complete urinary continence rate on the day of catheter removal and 1 month, 6 months, and 24 months after surgery;the total incidence of complications at each follow-up time point after surgery;

Countries

China

Contacts

Public ContactJun Pan

Guangdong Provincial Hospital of Chinese Medicine

dxcmnwk@126.com+86 20 3931 8781

Outcome results

None listed

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