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Clinical Trials/EUCTR2011-001819-30-DE
EUCTR2011-001819-30-DE
Active, not recruiting
Not Applicable

Detection of non-muscle invasive bladder cancer using PVP-Hypericin (Vidon®) fluorescence cystoscopy (Hypericin PDD)

Sanochemia Pharmazeutika AG0 sites220 target enrollmentJuly 18, 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suspected non-muscle invasive (superficial) bladder cancer
Sponsor
Sanochemia Pharmazeutika AG
Enrollment
220
Status
Active, not recruiting
Last Updated
11 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 18, 2011
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients who have given their signed declaration of consent and data
  • protection declaration
  • 2\. Males and females aged \= 18 years
  • 3\. Patients scheduled for transurethral resection of the bladder of a suspected bladder
  • cancer based on recent findings in cystoscopy that have to be diagnosed at the
  • respective study site prior to Visit 1
  • 4\. Patients including multiple bladder tumours or suspicious lesions
  • 5\. Patients with initial and/or recurrent bladder cancer
  • 6\. Patients with adequate renal and hepatic function according to the
  • investigator

Exclusion Criteria

  • 1\. Intravesical BCG (Bacillus Calmette\-Guérin) instillation \= 6 months
  • 2\. Intravesical Mitomycin instillation \= 3 months
  • 3\. Patients at high risk of suffering extensive bladder inflammation
  • 4\. Recent bladder surgery (resection) \= 3 months
  • 5\. Patients with symptoms and signs of urinary tract infection, e.g.
  • moderate or severe leukocyturia, dysuria, alguria, urgency, frequency,
  • polyuria, offensive urine, cloudy urine, significant bacteriuria (\= 100000
  • CFU/mL), positive urine culture, asymptomatic bacteriuria, suprapubic
  • tenderness, pain or pressure, flank or back pain, fever \= 38°C,
  • costovertebral angle tenderness

Outcomes

Primary Outcomes

Not specified

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