Skip to main content
OpenTrials
Completed

NCT Number: NCT00577785

Study to Obtain Full Thickness Bladder Tissue From Subjects Undergoing Cystectomy Surgery

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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Southern California

Los Angeles, California, 90033, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

tissue procurement

Other

No intervention. Tissue procurement study.

Primary outcomes

  1. Evaluation of bladder tissue from patients underogoing radical cystectomy

    Time frame: ongoing throughout study

Sponsors and collaborators

Lead sponsor

Tengion

Industry

Registry information

Official study title

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

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Dec 20, 2007
Registry last updated
Dec 22, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.