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Not yet recruitingNCT07112846CRIUSUpdated Aug 8, 2025

Prospective Clinical Registry for Evaluation of Exanthematous Infections and Coinfections

An observational study in Exanthema, Dengue Fever and Chikungunya, sponsored by Hospital Israelita Albert Einstein. Not yet recruiting. Open to participants aged Up to 18 Years. Per ClinicalTrials.gov, last updated 2025-08-08.

Sponsored by Hospital Israelita Albert Einstein · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2026, 4 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
830
Ages
Up to 18 Years
Sex
All
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Study 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.

02

Conditions studied

  • Exanthema
  • Dengue Fever
  • Chikungunya
  • Measles
  • Rubella

Keywords

  • exanthema
  • dengue fever
  • Chikungunya
  • measles
  • rubella
  • epidemiology
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In context

Exanthema

68 studies on the registry are indexed under Exanthema; 11 are open to participants now.

This study's planned enrollment of 830 is above the median of 71 across 18 observational studies indexed under Exanthema.

Browse Exanthema studies →

Lead sponsor

Hospital Israelita Albert Einstein is the lead sponsor of 147 studies on the registry; 32 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Up to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Participants without symptoms suspicious for the diseases presented.

Individuals with confirmed cases of the aforementioned infections prior to recruitment.

Individuals who, even presenting the symptoms described in the inclusion criteria, did not have samples collected for viral panel testing.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

-

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
830 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. Prevalence of positive infections for one or more infectious diseases (rubella, measles, dengue, and Chikungunya)

    Prevalence of positive infections for one or more infectious diseases (rubella, measles, dengue, and Chikungunya)

    Time frame: From enrollment to the end of follow-up (30 days).

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 8, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07112846
Responsible party
Sponsor
First posted
Aug 8, 2025
Start date
Sep 1, 2025 (estimated)
Primary completion
Jun 30, 2026 (estimated)
Completion
Jun 30, 2026 (estimated)
Last update
Aug 8, 2025

Study contacts

Henrique R A da Fonseca, PhD
Contact
henrique.fonseca@einstein.br
+551121511233
Karina Tozatto Maio, MD, PhD
Contact
karina.maio@einstein.br
+551121511233

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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Discussion

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