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Early Detection of Prostate Cancer by FACS

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00524823
Acronym
FACS
Enrollment
40
Registered
2007-09-05
Start date
2007-08-31
Completion date
Unknown
Last updated
2007-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperplasia, Prostate Cancer

Keywords

Prostate Cancer, Hyperplasia - BPH, FACS, Prostate Cancer, Hyperplasia - BPH, Malignancy

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.

Interventions

None listed

Sponsors

Ziv Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
DEFINED_POPULATION
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
60 Years to 90 Years
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. \-

Countries

Israel

Contacts

Primary ContactNina Kucherski, MD
050-8434041
Backup ContactYihia Johari, MD
050-8434094

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026