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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05770336
Other study ID # LONG-COVID
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 9, 2022
Est. completion date November 30, 2022

Study information

Verified date March 2023
Source IRCCS San Raffaele
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the project is to identify the prevalence and characteristics of long-term cardiovascular changes in Covid-19 infection.


Description:

In the follow-up of patients with Covid-19 infection, persistence of cardiovascular symptoms is common. Studies of the acute phase of Covid-19 infection have shown a significant prevalence of acute myocardial damage (15-44%), and imaging studies have confirmed the presence of structural changes in the pericardium and myocardium several months after the acute phase. The aim of the project is to identify the prevalence and characteristics of long-term cardiovascular changes in Covid-19 infection. The study is a continuation of the project "Registry "CARDICoVRISK"" which collected data on cardiovascular changes during the acute phase and shortly after the acute phase. The study design is retrospective observational. The study plans to enroll 240 patients hospitalized during the acute phase of COVID-19 infection. Patients will be collected at three separate centers. Enrolled patients will undergo a baseline evaluation by history, physical examination, laboratory tests, ECG, 6-minute walking test and echocardiogram. If alterations in left ventricular or right ventricular systolic function are found, as per the standard clinical approach, a cardiac MRI examination will be evaluated. Identification of patients with cardiac changes is of paramount importance as they may benefit from early initiation of cardioprotective therapy and may need different follow-up strategies.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date November 30, 2022
Est. primary completion date November 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Patient with previous hospitalization for Covid-19 infection confirmed by pharyngeal molecular swab - Adult patients between 18 and 90 years of age - Signature of informed consent Exclusion Criteria: - Patient with poor echocardiographic acoustic window impairing the performance of the examination - Patients with atrial fibrillation - Patients with ischemic or nonischemic heart disease with known decreased left ventricular systolic function

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy IRCSS San Raffaele Milan

Sponsors (2)

Lead Sponsor Collaborator
IRCCS San Raffaele Rete cardiologica IRCCS

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Identify the long-term myocardial damage and compare it with the prevalence and extent of acute myocardial damage. The main purpose of this study is to identify the long-term myocardial damage and compare it with the prevalence and extent of acute myocardial damage. The anatomical and functional substrates of cardiovascular manifestations will be analyzed by basic and advanced echocardiographic technologies 9 months
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