High risk human papillomavirus detection in semen

High risk human papillomavirus detection in semen - Semen study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON34492

Enrollment

200

Registered

2010-12-13

Start date

2011-10-01

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

HPV Human papillomavirus

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Male 18 years of age or older Sufficient knowledge of the Dutch or English language Signed informed consent

Exclusion criteria

Exclusion criteria: withdrawal of the informed consent

Design outcomes

Primary

Measure	Time frame
Endpoint is the HPV PCR outcome; i.e., presence or absence of hrHPV DNA in semen.	—

Secondary

Measure	Time frame
Evaluate the presence of flat penile lesions and the association with the prevalence of infection with human papillomavirus (HPV) in semen.	—

Countries

Netherlands

Outcome results