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Clinical Trial Summary

To compare the toxicity and efficacy of the combination of BCG and interferon alpha to standard dose and low dose BCG alone in high risk superficial bladder cancer


Clinical Trial Description

140 eligible patients with high risk superifical bladder cancer would be randomised to receive standard dose BCG, low dose BCG or the combination of low dose BCG and interferon alpha in a schedule of "6+3" weekly intravesical instillations. Patients would be closely monitored with cystoscopy and urine cytology and intravenous urograms when indicated. Pre-and post-instillation urine samples would be collected for cytokine analysis. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00330707
Study type Interventional
Source National University Hospital, Singapore
Contact
Status Completed
Phase Phase 2/Phase 3
Start date October 1995
Completion date June 2005

See also
  Status Clinical Trial Phase
Completed NCT01803295 - Pre-TURBT TC-3 Gel Intravesical Instillation in NMIBC N/A
Completed NCT02214602 - Value of Immediate Post-operative Intravesical Epirubicin in Intermediate&High Risk Non Muscle Invasive Bladder Cancer Phase 4