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Prospective Clinical Registry for Evaluation of Exanthematous Infections and Coinfections

Prospective Clinical Registry for Evaluation of Exanthematous Infections and Coinfections

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07112846
Acronym
CRIUS
Enrollment
830
Registered
2025-08-08
Start date
2025-09-01
Completion date
2026-06-30
Last updated
2025-08-08

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

Conditions

Chikungunya, Dengue Fever, Exanthema, Measles, Rubella

Keywords

exanthema, dengue fever, Chikungunya, measles, rubella, epidemiology

Brief summary

Exanthematous fevers are a global public health problem. The spread of arboviruses due to various factors, including climate change, has resulted in major epidemics such as the one that occurred in Brazil in 2024, representing an extremely concerning scenario from both epidemiological and healthcare perspectives. In addition to this, the reemergence of childhood exanthematous diseases in several countries, including Brazil, is alarming and occurs due to declining vaccination coverage and increased migratory movements. These diseases present overlapping clinical symptoms, and their differential diagnosis is often challenging, which, in a context of dengue and Chikungunya epidemics like the current one, may lead to underreporting of diseases such as measles and rubella. This project aims to build a prospective registry of the occurrence of dengue, Chikungunya, measles, and rubella in various healthcare centers in Brazil, in order to better understand the epidemiological scenario, identify clinical variables associated with different diagnoses, and describe healthcare bottlenecks that may hinder proper reporting and identification of these diseases.

Interventions

None listed

Sponsors

Hospital Israelita Albert Einstein
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
No

Inclusion criteria

Individuals from newborns (zero years old) to 18 years of age, of both sexes. Suspected individuals with the following criteria: Measles: Presenting fever and rash associated with cough and/or runny nose and/or conjunctivitis, regardless of age or vaccination status; Rubella: Presenting fever, rash, and lymphadenopathy, regardless of age or vaccination status; Dengue and Chikungunya: Presenting myalgia, arthralgia, headache, retro-orbital pain, nausea, vomiting, rash, petechiae, positive tourniquet test, or leukopenia and/or lymph node enlargement; Individuals who, meeting the above criteria, underwent sample collection for viral panel testing for the differential diagnosis of exanthematous diseases.

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of positive infections for one or more infectious diseases (rubella, measles, dengue, and Chikungunya)From enrollment to the end of follow-up (30 days).Prevalence of positive infections for one or more infectious diseases (rubella, measles, dengue, and Chikungunya)

Contacts

Primary ContactHenrique R A da Fonseca, PhD
henrique.fonseca@einstein.br+551121511233
Backup ContactKarina Tozatto Maio, MD, PhD
karina.maio@einstein.br+551121511233

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026