Early Detection of Prostate Cancer by FACS

Sponsor
Ziv Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT00524823
Collaborator
(none)
40
1

Study Details

Study Description

Brief Summary

Early detection of prostrate cancer and development of metastases. The research will attempt to match the SCM test (structuredness of the cytoplasmic matrix) in lymphocytes as an early cancer detection test using Florescent Activated Cell Sorting (FACS) as a replacement for the CellScan instrument. The test is based on measurement of cellular changes in response to the specific prostate antigen, PSA.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    40 participants
    Observational Model:
    Defined Population
    Time Perspective:
    Prospective
    Study Start Date :
    Aug 1, 2007

    Arms and Interventions

    Arm Intervention/Treatment
    1

    10 diagnosed men in age 60 - 90 with Prostate Cancer

    2

    10 patients with benign growth

    3

    10 health volunteers

    4

    10 patients diagnosed with other cancer

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      60 Years to 90 Years
      Sexes Eligible for Study:
      Male
      Accepts Healthy Volunteers:
      Yes
      Inclusion Criteria:

      Experimental group : Males between the ages of 60-90 years, with medical diagnosis of prostate cancer according to both clinical and hematological examinations, before receiving any medical treatment.

      Control Group 1: Males between the ages of 60-90 years, with diagnosed benign prostate hyperplasia -BPH.

      Control Group 2: Males between the ages of 60-90 years, medically diagnosed as healthy.

      Control Group 3: Males between the ages of 60-90 years, medically diagnosed with another form of cancer, not prostate.

      Exclusion Criteria:

      Experimental group: Other known cancer or systemic infection. Control Group 1: Other known cancer or systemic infection. Control Group 2:Past hematological disorders nor cancer growth history. other known systemic infection, nor urinary tract infection. Patients hospitalized for orthopedic injuries of any type who are otherwise free of urinary tract infections.

      Control Group 3:Other known systemic infection, nor urinary tract infection.

      -

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Urology Department, Ziv Medical Center Safed Israel 20100

      Sponsors and Collaborators

      • Ziv Hospital

      Investigators

      • Principal Investigator: Nina Kucherski, MD, Ziv Medical Center

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00524823
      Other Study ID Numbers:
      • HP 7-251 S
      First Posted:
      Sep 5, 2007
      Last Update Posted:
      Sep 5, 2007
      Last Verified:
      Aug 1, 2007

      Study Results

      No Results Posted as of Sep 5, 2007