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Clinical Trials/NCT00577785
NCT00577785
Completed
Not Applicable

A Multi-Center Study to Obtain Full Thickness Bladder Tissue Specimen From Subjects Undergoing Cystectomy Surgery

Tengion1 site in 1 country52 target enrollmentAugust 2007
ConditionsCystectomy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cystectomy
Sponsor
Tengion
Enrollment
52
Locations
1
Primary Endpoint
Evaluation of bladder tissue from patients underogoing radical cystectomy
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

The objective of this study is to obtain bladder tissue specimens from patients otherwise undergoing cystectomy for use in research and training of personnel at Tengion, Inc.

Registry
clinicaltrials.gov
Start Date
August 2007
End Date
January 2009
Last Updated
15 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Tengion

Eligibility Criteria

Inclusion Criteria

  • Subjects 18 to 90 years and undergoing a cystectomy surgery
  • Willing and able to give signed informed consent

Exclusion Criteria

  • Known active infection
  • Known colonization with MRSA or VRE
  • Receipt of blood or blood products for transfusion during the previous 3 months

Outcomes

Primary Outcomes

Evaluation of bladder tissue from patients underogoing radical cystectomy

Time Frame: ongoing throughout study

Study Sites (1)

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