Aberrant Gene Expression Prostate Carcinoma

NCT ID: NCT00868803

Last Updated: 2025-06-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

5000 participants

Study Classification

OBSERVATIONAL

Study Start Date

1995-04-30

Study Completion Date

2030-04-30

Brief Summary

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The goal of the study is to gain a better understanding of the molecular changes responsible for causing prostate cancer and that examination of tissue and blood samples will help in the development of improved screening and therapeutic approaches.

Detailed Description

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The goal of this study is to identify novel genetic elements that are aberantly expressed throughout prostatic neoplastic progression. The approaches proposed exploit the known familial arm of prostatic cancer, using established molecular genetic approaches, and extend these studies to sporadic prostatic cancer using a novel technique of differential display. Application of the latter technique to colon cancer in the American population establishes this tumor type as a high priority for scientific investigation and this study is part of an initiative to address this problem. Presently the studies in the field of prostate are under-represented. The collection of tissue samples from patients diagnosed with prostate cancer. Patients will also provide a blood sample at the time of their surgery and potentially post-op from 6 mos to 5 years. Samples will also be obtained from patients who's biopsy turns out to be non-prostate cancer. These samples will be obtained shortly following the biopsy out to 6 months after the biopsy.

Conditions

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Prostate Cancer

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Diagnosed prostate cancer undergoing prostatectomy
* Suspicion of prostate cancer undergoing biopsy - negative biopsy
* Health volunteer (control group) - blood sample for PSA
Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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Lahey Clinic

OTHER

Sponsor Role lead

Responsible Party

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Linda Topjian

study coordinator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kimberly R Christ, PhD

Role: PRINCIPAL_INVESTIGATOR

Lahey Clinic

Locations

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Lahey Clinic

Burlington, Massachusetts, United States

Site Status

Countries

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United States

Other Identifiers

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LCID1995-014

Identifier Type: -

Identifier Source: org_study_id

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