Recruiting

Observational Study

Sponsor:

LifeBridge Health

Code:

NCT04493307

Conditions

COVID-19

Eligibility Criteria

Sex: All

Age: 3+

Healthy Volunteers: Not accepted

Interventions

Phlebotomy

Study Details

Brief summary:

Coronavirus disease 2019 (COVID-19), a viral respiratory illness caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has been shown to predispose patients to thrombotic diseases (venous and arterial) with reported rates in hospitalized patients between 17-40%. The influence of SARS-CoV-2 infection on the coagulation is hypothesized to be regulated by platelet activation, proinflammatory cytokines, endothelial cell injury and stasis. The elevated levels of d-dimer and fibrinogen and clinical signs of organ damage point to a significant hypercoagulable state. The latter induces a high risk for micro-thrombi and multi-organ ischemia. Therefore, early detection and a comprehensive understanding of the influence of the virus on the coagulation and platelet pathways are essential to address this epidemic. It is critical at this time to make all efforts possible to optimize our available technology to care for COVID-19 patients who are at risk for thrombotic disease through appropriate choice, dosing, and laboratory monitoring of antithrombotic therapy.

The investigators hypothesize that COVID-19 is a heightened prothrombotic/hypercoagulability state that can be characterized using platelet function testing and thrombelastography. More information is required to study the effect of COVID-19 on coagulation and platelet pathways to develop effective antithrombotic treatment strategies.

This is a multi-center center, non-interventional study enrolling patients who are COVID-19 positive or who have tested negative showing indication of the disease (high D-dimer and positive lung imaging). The study specific laboratory assessments will be obtained at baseline (closest to time of hospitalization), Day 3, and Day 8 from baseline and at hospital discharge. Laboratory measurements for TEG 6S , platelet aggregation, T-TAS, urinary thromboxane, genotyping, serum and plasma biomarkers will be analyzed . In-hospital and clinical follow-up data will be entered into a COVID registry Patients will be followed for clinical events during hospitalization, and up to 6 months after discharge.

Patients (n=100) hospitalized with at least one of the following will be enrolled.

1. With a confirmed diagnosis of COVID-19 infection using a positive RT- PCR or a positive IgG antibody test prior to or during hospitalization or
2. With a negative COVID-19 RT-PCR test but with symptoms of possible

COVID-19 infection and:

1. an elevated D-dimer and/or
2. positive imaging results showing unilateral or bilateral pneumonia or ground-glass opacity in lungs.

Conditions

COVID-19

Study ID

NCT04493307

Start date

Jun 30, 2020

Status verified date

Jul, 2020

Completion date

Jun, 2021

Anticipated

Primary completion date

Feb, 2021

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 3+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • · Confirmed diagnosis of COVID-19 infection using a positive RT-PCR or a positive IgG antibody test prior to or during hospitalization or,

· With a negative COVID-19 RT-PCR test but with symptoms of possible COVID-19 infection and:
  • elevated D-dimer and/or
  • positive imaging results showing unilateral or bilateral pneumonia or ground-glass opacity in lungs · The subject or legal authorized representative able to read and sign an informed consent document including authorization permitting release of personal health information approved by the investigator's Institutional Review Board (IRB).

Exclusion Criteria:

Subjects will be excluded from entry if ANY of the criteria listed below are met:

  • Less than 3 years of age
  • Subject is pregnant
  • Active treatment for cancer
  • History of long-term use of immunosuppressive agents
  • History of severe chronic respiratory disease and requirement for long-term oxygen therapy
  • Patients undergoing hemodialysis or peritoneal dialysis
  • Patients on full dose anticoagulant at the time of enrollment
  • Any condition unsuitable for the study as determined by investigators

Study Design

Enrollment

100 participants

Anticipated

Interventions and Outcome Measures

Interventions

Phlebotomy

Serial assessment of hemostasis by blood and urine collection

Primary outcome measure

  • Frequency of Hypercoagulability as measured by thromboelastography measured by TEG and platelet aggregation. [ Time Frame: up to day 8 ]

Central Contacts and Locations

Central contacts

Locations

Sinai Center for Thrombosis Research

Recruiting

Baltimore, Maryland, United States, 21215

Contacts

Principal Investigator:

Paul A Gurbel, MD

More Information

Sponsor

LifeBridge Health

Last update posted

Oct 22, 2020

Last verified

Jul, 2020

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by LifeBridge Health on 2020-10-22.