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Surgical Standarization and Treatment Assessment of Laparoscopic Radical Cystectomy-Bladder Reconstruction

Surgical Standarization and Treatment Assessment of Laparoscopic Radical Cystectomy-Bladder Reconstruction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10001003
Enrollment
Unknown
Registered
2010-08-28
Start date
2008-01-24
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Muscle-invasive bladder cancer

Interventions

Experimental Group:Laparoscopic Radical Cystectomy with Orthotopic Ileal Neobladder
Control Group:Open Radical Cystectomy with Orthotopic Ileal Neobladder

Sponsors

Sun Yat-sen Memorial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Muscle-invasive bladder cancer (T2-T4a, N0-x, M0); Multiple recurrent non-muscle invasive bladder cancer; G3 non-muscle invasive bladder cancer; multiple carcinoma in situ; extensive papillary disease can not be controlled by conservasive treatment; recurrent or unresponse after bladder-preserving treatment; Non-transitional cell carcinoma in bladder; 2. Intraabdomial pressure > 60cm H2O preoperatively; 3. Normal function of urethral sphincter; 4. Zubrod-ECOG-WHO (ZPS) Grade: 0-2; Karnofsky Perfromance Status (KPS) >=60; 5. Patients provided voluntary informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Patient with distant metastasis disease; 2. Tumor in urethral (Tumor locate below bladder neck in male, and trigone of bladder in female); 3. Co-exist disease which may affect intraabdominal pressure (esophageal hiatal hernia, abdominal hernia, abnormal abdominal or pelvic straining); 4. Stricture of anterior urethra; 5. Co-exist intestinal disease; 6. Previous resection of small intestine; 7. Severe heart insufficiency, decompensated pulmonary, liver, renal functons, or other severe systemic disease; 8. Stress incontinence in femal or previous bladder nek suspension; 9. Other situation which was recognized should be excluded by the researcher.

Design outcomes

Primary

MeasureTime frame
Oncological Outcome in 5 years;

Secondary

MeasureTime frame
Operative Time, Estimated Blood Loss, Transfution;Sexual Function at 1-year follow up;Postoperative early and late complications;Neobladder Function at 1-year follow u;

Countries

China

Contacts

Public ContactJian HUANG
yehjn@yahoo.com.cn+86 20 81332336

Outcome results

None listed

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