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Clinical Trials/NCT01819740
NCT01819740UnknownNot Applicable

Analysis of a New Biomarker for Prostate Cancer Diagnosis

Corporacion Parc Tauli1 site in 1 country28 target enrollmentStarted: April 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
28
Locations
1
Primary Endpoint
substance "HEM" concentration in seminal plasma (mEq/L measured by spectro-photometry

Study Overview

Brief Summary

The aim of our study is to determine if the levels of the "HEM" substance in seminal plasma are associated with the presence of prostate cancer in transrectal prostate biopsy.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
45 Years to 75 Years (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Clinical or laboratory suspected of prostate cancer

Exclusion Criteria

  • Inability to ejaculate

Outcomes

Primary Outcomes

substance "HEM" concentration in seminal plasma (mEq/L measured by spectro-photometry

Time Frame: 1 hour

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Corporacion Parc Tauli
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

MIRIAM BARRIO MUÑOZ

UROLOGY RESIDENT

Hospital de Sabadell

Study Sites (1)

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