- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07007377
- Original Trial
Can the Ergometric Test in Flu-like Syndrome Help in the Outcome Analysis of Unvaccinated Patients
May 15, 2026 updated by: Pedro Gabriel Senger Braga, University of Sao Paulo
During the flu-like syndrome, the cardiovascular risk is increased, especially in the elderly.
Understanding whether blood pressure assessment during an exercise test can aid in the understanding of patient outcomes, thereby improving prognostic ability in clinical practice, is the focus of the present study.
Therefore, the aim of this study is to evaluate the hemodynamic response of adults with flu-like symptoms, both vaccinated and unvaccinated, and to conduct a 30-day follow-up for assessment.
Patients who are indicated for an ergometric test and present with flu-like syndrome will be selected.
We will inquire about their vaccination history and perform the ergometric test to evaluate test duration, arrhythmias, and ischemias
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
62
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
São Paulo
-
São Paulo, São Paulo, Brazil, 05021010
- Clínica Pró-Coração
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Adults with flu symptoms, which were vaccinated or not.
Description
Inclusion Criteria:
- flu-symptoms
Exclusion Criteria:
- recent orthopedic surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Vaccinated
Vaccinated subjects
|
Follow-up
|
|
Non-vaccinated
Non-vaccinated subjects
|
Follow-up
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Can the ergometric test in flu-like syndrome help in the outcome analysis of unvaccinated patients?
Time Frame: 1 month
|
The investigators will analyze whether different responses to exertion, such as blood pressure disorders, are more evident in individuals with or without symptoms who have or have not been vaccinated.
|
1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Symptoms
Time Frame: 7 and 14 days after treadmill exercise test
|
The investigators will document whether the symptoms are present or not.
|
7 and 14 days after treadmill exercise test
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2025
Primary Completion (Actual)
August 29, 2025
Study Completion (Actual)
December 5, 2025
Study Registration Dates
First Submitted
March 27, 2025
First Submitted That Met QC Criteria
June 2, 2025
First Posted (Actual)
June 5, 2025
Study Record Updates
Last Update Posted (Actual)
May 19, 2026
Last Update Submitted That Met QC Criteria
May 15, 2026
Last Verified
June 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Clínica Pró-Coração
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Data protection
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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