Test Semiquantitative Prostate Specific Antigen (PSA)

NCT00853710 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 94

Last updated 2025-11-20

No results posted yet for this study

Summary

The aim of the study is to compare the diagnostic performances of a simple and rapid PSA assay on whole blood to the standard plasma PSA assay.

Conditions

Interventions

OTHER

PSA assay

rapid prostate specific antigen assay.

Sponsors & Collaborators

  • Institut Curie

    lead OTHER

Principal Investigators

  • Dominique BELLET, Pr · Institut Curie

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-03-31
Primary Completion
2009-07-31
Completion
2009-07-31

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00853710 on ClinicalTrials.gov