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Not yet recruiting NCT05983679

Prevalence of Sexually Transmitted Infections (STIs) and Coinfections in the General Population

Observational HIV Infections

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 →
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

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗