Prevalence of Sexually Transmitted Infections (STIs) and Coinfections in the General Population
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Blood sample.
- Who it may be relevant to
- Registry conditions: HIV Infections. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Prevalence of Sexually Transmitted Infections (STIs) and Co-infections in the General Population
Overview
Prevalence of Sexually Transmitted Infections (STIs) and co-infections in the general population
Interventions
- Diagnostic test Blood sample
Blood sample
Primary outcome measures
- The prevalence of each STI will be assessed by the participant's positive or negative status for each pathogen, determined by the following screening tests: [Time frame: 3 years]
Eligibility criteria
Inclusion criteria
- Subject, male or female, 18 years of age or older
- Subject capable of understanding the purpose of the research having given their free and informed written consent
- Subject presenting to the laboratory for a biological examination
- Affiliated subject or beneficiary of a social security scheme
Exclusion criteria
\- Protected subject: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT05983679 · PREMINF