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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02070575
Other study ID # 14-041
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 20, 2014
Est. completion date October 18, 2023

Study information

Verified date October 2023
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to investigate if a new blood test looking at PSA and a group of PSA related proteins in a patient's blood can indicate which men after surgery with a rising PSA could benefit from treatment, and/or indicate which men are at higher risk for recurrence before initial treatment is given.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date October 18, 2023
Est. primary completion date October 18, 2023
Accepts healthy volunteers No
Gender Male
Age group 30 Years and older
Eligibility Inclusion Criteria: - All patients treated with radical prostatectomy that develop a rising serum PSA = 0.05ng/ml and have not received any kind of additional therapy. - Patients who have had additional therapy post radical prostatectomy are eligible for this study if =1 year has passed since treatment and the patient develops a rising serum PSA =0.05ng/ml. Exclusion Criteria: - Previous additional therapy for prostate cancer, less than 1 year ago - No evidence of rising PSA - Patients unwilling to undergo venesection

Study Design


Related Conditions & MeSH terms


Intervention

Other:
blood draw
Venous blood will be collected in an EDTA Vacutainer tubeup to 10 mL and will be immediately put on ice. This sample may be drawn as a stand-alone blood draw. Samples will be centrifuged at 1900g (3000-3200 RPM) for 15 Minutes and the serum aliquoted into freezer vials and stored at -80°C until analysis. In addition patients who have not received treatment for biochemical recurrence after their first draw are eligible for subsequent draws to determine the reproducibility of the test over time.

Locations

Country Name City State
United States Memorial Sloan Kettering Cancer Center New York New York

Sponsors (1)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary profile of a panel of kallikrein related serine proteases in the blood of patients that present with biochemical recurrence after radical prostatectomy. 2 years
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