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Clinical Trials/NCT00524823
NCT00524823
Unknown
Not Applicable

Early Detection of Prostate Cancer by FACS

Ziv Hospital1 site in 1 country40 target enrollmentAugust 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Ziv Hospital
Enrollment
40
Locations
1
Last Updated
18 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
August 2007
End Date
TBD
Last Updated
18 years ago
Study Type
Observational
Sex
Male

Investigators

Sponsor
Ziv Hospital

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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