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Prospective Hospital Registry of Patients With Suspected or Confirmed Coronavirus Infection (COVID-19) and Community-acquired Pneumonia

Prospective Hospital Registry of Patients With Suspected or Confirmed Coronavirus Infection (COVID-19) and Community-acquired Pneumonia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04522076
Acronym
TARGET-VIP
Enrollment
1130
Registered
2020-08-21
Start date
2020-04-06
Completion date
2026-12-31
Last updated
2025-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID 19

Brief summary

Coronavirus-2019 disease (COVID-19) and community-acquired pneumonia are significant problems of modern medicine. Pneumonia is the most common severe complication of COVID-19. But at the same time, COVID-19 is not the only cause of community-acquired pneumonia. Moreover, pneumonia is only one of the numerous possible severe complications of COVID-19. Medical centers specialized for the hospital treatment of patients with severe COVID-19 and community-acquired pneumonia were organized in different regions of Russia during coronavirus pandemic-2020. The indications for hospitalization to one of these centers based in the National Medical and Surgical Center (NMSC) are: confirmed or suspected severe COVID-19 or community-acquired pneumonia. A prospective medical registry of such patients hospitalized to NMSC, is intended to analyze and compare their clinical and instrumental data, co-morbidity, treatment, short-term and long-term outcomes in real clinical practice. Stage 1. Hospital treatment in NMSC Duration of this stage: from the date of admission to the hospital up to the date of discharge from the hospital / or up to the date of death during the reference hospitalization. The date of admission to the hospital will be the date of enrollment to the study. Evaluation of electronic health record data using the Medical Information System (MIS). Assessment of the outcomes of the hospital phase (discharge from the hospital, death) and significant events (acute respiratory and pulmonary failure, requiring mechanical ventilation; cardiovascular events - myocardial infarction, cerebral stroke, acute heart failure, paroxysmal heart rhythm disturbances, bleedings, thrombosis of large vessels and thromboembolic complications). A survey of patients to clarify data on risk factors, somatic diseases, and drug therapy before hospitalization. COVID-19 was diagnosed when severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection was confirmed by Polymerase chain reaction (PCR). Pneumonia was confirmed according to computerized tomography (CT) data. Stage 2. Prospective outpatient follow-up for 24 months Duration of this stage: 24 months after discharge from the hospital This work will be delivered by investigators from the National Medical Research Center for Therapy and Preventive Medicine. Evaluation of long-term outcomes and events among residents of Moscow and the Moscow Region according to a patient survey (contact by phone for 30-60 days, 6 months, 12 and 24 months after discharge from the hospital) and medical records.

Interventions

None listed

Sponsors

National Medical and Surgical Center named after N.I. Pirogov of the Ministry of Healthcare of the Russian Federation
CollaboratorUNKNOWN
National Research Center for Preventive Medicine
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients hospitalized to the National Medical and Surgical Center named after N.I.Pirogov of the Ministry of Health of Russia (NMSC) with suspected or confirmed COVID-19 or community-acquired pneumonia. 2. Age 18 years and older. 3. Permanent residency in Russia.

Exclusion criteria

1. Permanent residency outside of Russia. 2. The patient's refusal to participate in the study.

Design outcomes

Primary

MeasureTime frame
Overall survivalfrom admission to discharge or death during reference hospitalization, assessed up to 90 days
Time to all-cause mortality, nonfatal myocardial infarction, nonfatal cerebral stroke, and coronary or carotid revascularizationfrom discharge up to two years after reference hospitalization
Time to all-cause mortality or Artificial Pulmonary Ventilation (APV)from admission to discharge or death during reference hospitalization, assessed up to 90 days

Secondary

MeasureTime frameDescription
Proportion of patients with severe pneumoniafrom admission to discharge or death during reference hospitalization, assessed up to 90 daysDamage area \>50% according to the computer tomography data at any time point during hospitalization
Proportion of patients with low oxygen saturation valuefrom admission to discharge or death during reference hospitalization, assessed up to 90 daysSpO2 \<90% - at any point during hospitalization
Proportion of patients with Hb <90 g/l (9.0 g/dl) at any point during hospitalizationfrom admission to discharge or death during reference hospitalization, assessed up to 90 days
Proportion of patients hospitalized or transferred to Intensive Care Unit (ICU)from admission to discharge or death during reference hospitalization, assessed up to 90 days
Overall survivalfrom discharge up to two years after reference hospitalization
Time to nonfatal myocardial infarction, nonfatal cerebral stroke, and coronary or carotid revascularizationfrom discharge up to two years after reference hospitalization
Time to pneumonia/recurrent pneumoniafrom discharge up to two years after reference hospitalizationIn patients with pneumonia during reference hospitalization time to recurrent pneumonia. In patients without pneumonia during reference hospitalization - time to first pneumonia
Time to primary or recurrent coronavirus infection disease (COVID-19)from discharge up to two years after reference hospitalizationIn patients without COVID-19 - time to primary diagnosis and in patients with COVID-19 - time to recurrent event

Other

MeasureTime frameDescription
proportion of patients with nonfatal cerebral strokefrom admission to discharge or death during reference hospitalization, assessed up to 90 days
thromboembolic eventsfrom admission to discharge or death during reference hospitalization, assessed up to 90 daysproportion of patients with thromboembolic events
proportion of patients with bleedingsfrom admission to discharge or death during reference hospitalization, assessed up to 90 days
Duration of Artificial Pulmonary Ventilationfrom admission to discharge or death during reference hospitalization, assessed up to 90 daysthe sum of the days when the patients required artificial pulmonary ventilation
Minimal value of oxygen blood saturation (SpO2) during the hospital stage.from admission to discharge or death during reference hospitalization, assessed up to 90 days
Minimal value of hemoglobin (Hb) during the hospital stagefrom admission to discharge or death during reference hospitalization, assessed up to 90 days
Rehospitalization due to pneumonia, COVID-19, flu and other acute respiratory infections (ARV)from discharge up to two years after reference hospitalizationproportion of patients with rehospitalization due to pneumonia, COVID-19, flu and other acute respiratory infections (ARV)
Hospitalization due to cardiovascular disease (CVD)from discharge up to two years after reference hospitalizationproportion of patients with hospitalization due to cardiovascular disease
time to Flu and other ARV (except COVID-19)from discharge up to two years after reference hospitalization
proportion of patients with nonfatal myocardial infarctionfrom admission to discharge or death during reference hospitalization, assessed up to 90 days

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026