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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05226416
Other study ID # ACTIV4
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 21, 2022
Est. completion date April 21, 2023

Study information

Verified date May 2023
Source Eurasian Association of Therapists
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Depersonalized multi-centered registry initiated to analyze dynamics of non-infectious diseases after SARS-CoV-2 infection in population of Eurasian adult patients.


Description:

Assessment of hospital course and health status during 3, 6, 12 months after discharge in COVID-19 patients in cohorts with comorbidities and without comorbidities. Evaluation of comorbidity impact to severity of novel coronavirus disease and comorbidity impact to demand for medical care.


Recruitment information / eligibility

Status Completed
Enrollment 3554
Est. completion date April 21, 2023
Est. primary completion date March 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Suspected or confirmed COVID-19 Exclusion Criteria: - Age under 18 years. - Refusal to be involved in study;

Study Design


Related Conditions & MeSH terms

  • Anemia
  • Arrythmia
  • Asthma
  • Atrial Fibrillation
  • Chronic Heart Failure
  • Chronic Kidney Diseases
  • Copd
  • Coronary Artery Disease
  • COVID-19
  • Diabetes Mellitus
  • DVT
  • Embolism
  • Heart Diseases
  • Heart Failure
  • Hypertensive Heart Disease
  • Ischemia
  • Ischemic Heart Disease
  • Ischemic Stroke
  • Kidney Diseases
  • Myocardial Infarction
  • Myocardial Ischemia
  • Myocarditis
  • Oncology
  • Overweight
  • Overweight and Obesity
  • Pulmonary Embolism
  • Renal Insufficiency, Chronic
  • Stroke

Locations

Country Name City State
Russian Federation Eurasian Association of Therapists Moscow

Sponsors (1)

Lead Sponsor Collaborator
Eurasian Association of Therapists

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary death for any cause rate of lethal outcomes From date of hospitalization until the date of first documented date of death from any cause, assessed up to 12 months
Primary hospitalization for any cause rate of hospitalization for any cause 12 months after discharge
Secondary onset of any disease diagnosed 1 year after discharge rate of patients with onset of any disease diagnosed 1 year after discharge 1 year after discharge
Secondary rate of demand for medical care number of patients seeking for health care after discharge 1 year after discharge
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