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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05078554
Other study ID # 8048
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 27, 2021
Est. completion date January 27, 2022

Study information

Verified date October 2021
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main objective of this study is to find out whether young MSM (men who have sex with men) believe it is important for their GP to be informed of their sexual orientation, in order to improve their clinical, especially with HPV vaccination. The secondary objective is to analyze the state of knowledge about the HPV vaccine and the value of HPV vaccine in this target population.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date January 27, 2022
Est. primary completion date January 27, 2022
Accepts healthy volunteers
Gender Male
Age group 18 Years to 26 Years
Eligibility Inclusion criteria: - Age: 18-26 years - Consultation at the HUS Cegidd as part of an STI screening - Subject who expressed no opposition to participating in the study Exclusion criteria: - Refusal of the patient to participate in the study - Subject who had already benefited from HPV vaccination (at least one dose) - Inability to give informed consent - Subject under safeguarde of justice - Subject under guardianship or under curatorship

Study Design


Locations

Country Name City State
France Service du Trait d'Union - Hôpitaux Universitaires de Strasbourg Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Retrospective descriptive study of vaccination against HPV (Human Papilloma Virus) in Alsace? Files analysed retrospectively from April 27, 2021 to January 27, 2020 will be examined]
See also
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Recruiting NCT05916911 - Evaluation Of The Efficacy Of The Combination Of GLIZIGEN® Oral Solution 1/Day And Vaginal Gel 1/Night For 2 Months In Patients With Cervical Intraepithelial Neoplasia Grade 1 (LSIL/CIN-1) Caused By High-Risk Human Papillomavirus (HPV-AR) Phase 4
Completed NCT01030562 - Immunogenicity of Off-Schedule Dosing of HPV Vaccine