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NCT00848289Active, not recruiting

Genetic Susceptibility to Bladder Cancer

Genetic Susceptibility to Bladder Cancer: A Molecular Epidemiology Approach

Source: ClinicalTrials.gov · Last updated 16 Jul 2026

Brief summary (registry, in English)

This clinical research study will identify biologic and lifestyle factors which increase a person's risk of developing specific cancer. Researchers propose to conduct a case-control study examining interindividual differences in susceptibility to tobacco carcinogenesis as predictors of bladder cancer risk. We will measure susceptibility to tobacco carcinogenesis and this will include studies of the genetic modulation of carcinogen activation and detoxification and of chromosome sensitivity to tobacco mutagens.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
6086 (actual)
First submitted
19 Feb 2009
Start date
10 Feb 1998
Primary completion date
1 Aug 2026
Lead sponsor
M.D. Anderson Cancer Center
NCT number
NCT00848289

What you commit to

  • Study type: Observational
  • Participants enrolled: 6086
  • From 10 Feb 1998 to the primary completion date, 1 Aug 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Subject has had prior treatment with systemic chemotherapy or radiotherapy in the past 6 months.

Other illness

  • Subject has been diagnosed with superficial or muscle-invasive bladder cancer more than twelve months ago.

Who the study is looking for

  • Subject has a histologically confirmed diagnosis of superficial or muscle-invasive bladder cancer
  • Subject is a Texas resident.
  • Subject can understand English or a qualified translator is available for the interview.
  • Subjects of any age, gender, or ethnicity are eligible to participate in the study.
  • Subject consents to participate in the study.

Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Baylor College of Medicine
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
MD Anderson Cancer Center
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.