NCT Number: NCT00373035
Biomarkers in Patients Undergoing Transrectal Ultrasound Prostate Biopsy
RATIONALE: Collecting and storing samples of blood and urine from patients with cancer to study in the laboratory may help doctors learn more about changes that may occur in DNA and identify biomarkers related to cancer.
PURPOSE: This laboratory study is looking at biomarkers in patients undergoing transrectal ultrasound prostate biopsy.
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Notify MeKey information
Conditions
Age range
18 year–120 year
Sex eligibility
Male
Study type
Observational
Primary location
SurroMed Incorporated, Menlo Park, California, United States
About this study
OBJECTIVES:
Primary
- Identify unique proteins or peptides that are associated with prostate cancer by comparing the proteomic or metabolomic analysis of serum, plasma, and urine from patients with histological evidence of prostate cancer to those without prostate cancer (after transrectal ultrasound prostatic biopsy).
Secondary
- Collect seminal fluid from a subset of patients to test the hypothesis that the fluid collected from the "target organ of injury" in prostate cancer will have a higher signal of proteins/peptides that are different from those without cancer and may help guide the identification of these differences in the serum, plasma, and urine.
OUTLINE: This is a pilot study.
Patients undergo collection of serum, plasma, and urine for biomarker/laboratory analysis. Samples are examined by proteomic/metabolomic analysis (by mass spectrometry) and immunoassays. Patients then undergo a transrectal ultrasonography prostatic biopsy.
PROJECTED ACCRUAL: A total of 60 patients will be accrued for this study.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
DISEASE CHARACTERISTICS:
- Indication for a transrectal ultrasonography prostatic biopsy (as part of normal patient care) due to elevated prostate-specific antigen, or abnormal digital rectal examination, or surveillance for prostate cancer
PATIENT CHARACTERISTICS:
- No prior or other concurrent malignancy except for curatively treated basal cell carcinoma of the skin
- No serious medical or psychiatric illness that would preclude informed consent
- No concurrent acute illness
PRIOR CONCURRENT THERAPY:
- No participation in another clinical trial within the past 30 days
- No more than one enrollment into this study
Treatment and study plan
immunological diagnostic method
Otherlaboratory biomarker analysis
Othermass spectrometry
OtherBiopsy
ProcedureUltrasound Imaging
ProcedurePrimary outcomes
-
Unique proteins or peptides associated with prostate cancer
Sponsors and collaborators
Lead sponsor
Wake Forest University Health Sciences
Other
Collaborators
- National Cancer Institute (NCI)
Registry information
Official study title
Biomarkers of Prostate Cancer
Important dates
- Study start
- 2006
- Primary completion
- 2006
- First posted
- Sep 7, 2006
- Registry last updated
- Jan 19, 2017
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.
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