WORLD HEART FEDERATION (WHF) COVID-19 and Cardiovascular Disease Survey

  • STATUS
    Recruiting
  • participants needed
    5200
  • sponsor
    Public Health Foundation of India
Updated on 19 February 2024
cardiovascular disease
cardiovascular complications
covid-19
cardiovascular complication

Summary

A global study for a better understanding of the cardiovascular conditions that increase the risk of developing severe COVID-19, and a better characterization of cardiovascular complications in hospitalized patients with COVID-19.

Description

COVID-19 may be cardiotropic in a subset of patients. Both acute and pre-existing CVD impact outcomes unfavorably. It is possible that one common CVD treatment, medications that impact ACE-2 function, may impact outcomes either favorably or unfavorably.

However, studies so far have, perforce, been conducted with important limitations (e.g. small numbers, limited geographical representation, lack of data standardization for risk factors and outcomes, limited measurement, lack of appropriate adjustment for important confounders, and missing data). Considering the high global prevalence of CVD and its risk factors (e.g. hypertension and diabetes) and the suggested link with COVID19 it is urgent to initiate more robust studies to clarify the many issues early reports have engendered. So that investigators will conduct a global study for a better understanding of the cardiovascular conditions that increase the risk of developing severe COVID-19, and a better characterization of cardiovascular complications in hospitalized patients with COVID-19.

Details
Condition Cardiovascular Disease, Covid 19
Age 18-100 years
Clinical Study IdentifierNCT04475471
SponsorPublic Health Foundation of India
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

All adults (as locally defined) with confirmed COVID-19 infection who are hospitalized are eligible

Exclusion Criteria

Patients for whom investigators are unable to obtain informed consent will be excluded
Patients who are unlikely to stay in the recruiting centre for 30 days (i.e. likely to be transferred)
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  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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