Recruiting

Coagulopathy

Sponsor:

University of Iowa

Code:

NCT05334615

Conditions

COVID-19

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

At the University of Iowa, the investigators led a multicenter randomized clinical trial comparing standard prophylactic dose to intermediate dose enoxaparin in hospitalized patients with COVID-19 (NCT04360824). As part of an exploratory biomarker component of this trial, blood samples were collected from hospitalized COVID-19 patients at enrollment and weekly for up to 30 days of hospitalization. The pilot results, as well as reports from other groups, demonstrate increased potential for thrombin generation in the plasma of COVID-19 patients. In particular, in the COVID-19 patient cohort enhanced thrombin generation potential persisted for at least 30 days of hospitalization. The investigators now propose to explore the mechanistic roles of activation of blood cells (such as platelets and neutrophils) and products of cellular activation as mediators of enhanced thrombin generation in patients with COVID-19. The study design will be a longitudinal cohort study, which will allow for the determination of the time course of enhanced thrombin generation potential in relation to clinical outcomes and changes in markers of cellular activation in serial samples obtained from COVID-19 patients for up to 3 years after infection with SARS-CoV-2. This study may provide clues to why a subset of COVID-19 patients present with late thrombotic complications even after apparent recovery from SARS-CoV-2 infection. An ongoing question in the field relates to the comparative prothrombotic effects of acute COVID-19 versus incidental SARS-CoV-2 infection versus acute infection with influenza viruses. Therefore, we will include three categories of hospitalized patients in this study: (1) acute COVID-19, (2) incidental COVID-19, and (3) acute influenza A or B. This project has a strong scientific rationale with direct clinical implications, especially given the emergence of SARS-CoV-2 variants such as delta and omicron that may prolong the pandemic and/or cause surges of COVID-19 in the coming months.

Conditions

COVID-19

Study ID

NCT05334615

Start date

Jan 21, 2022

Status verified date

Apr, 2025

Completion date

Dec 31, 2025

Anticipated

Primary completion date

Dec 31, 2025

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion criteria

Subjects must meet all inclusion criteria in one of the following three categories:

1. Acute COVID-19

  • Hospital admission for management of symptoms related to COVID-19
  • Laboratory confirmed infection with SARS-CoV-2 by either PCR or antigen testing within 4 weeks of hospital admission
  • Age ≥18 years
2. Incidental COVID-19

  • Hospital admission for indications unrelated to COVID-19 who are incidentally found to have infection with SARS-CoV-2
  • Age ≥18 years
3. Acute influenza

  • Hospital admission for clinical management of symptoms related to influenza
  • Laboratory confirmed infection with influenza A or influenza B within 4 weeks of hospital admission
  • Negative testing for SARS-CoV-2
  • Age ≥18 years

Exclusion criteria

  • Current pregnancy
  • Prisoner
  • History of a bleeding disorder
  • Active cancer

Study Design

Enrollment

180 participants

Anticipated

Interventions and Outcome Measures

Arms

Acute COVID-19

Hospital admission for management of symptoms related to COVID-19. Laboratory confirmed infection with SARS-CoV-2 by either PCR or antigen testing within 4 weeks of hospital admission.

Age ≥18 years.

Incidental COVID-19

Hospital admission for indications unrelated to COVID-19 who are incidentally found to have infection with SARS-CoV-2.

Age ≥18 years.

Acute influenza

Hospital admission for clinical management of symptoms related to influenza. Laboratory confirmed infection with influenza A or influenza B within 4 weeks of hospital admission.

Negative testing for SARS-CoV-2. Age ≥18 years.

Primary outcome measure

  • Thrombin generation [ Time Frame: 3 years ]
  • Blood cell activation [ Time Frame: 3 years ]
  • Cellular mediators of thrombin generation [ Time Frame: 3 years ]

Central Contacts and Locations

Central contacts

Locations

University of Iowa Health Care

Recruiting

Iowa City, Iowa, United States, 52242

Contacts

Principal Investigator:

Steven R Lentz, MD, PhD

More Information

Sponsor

University of Iowa

Last update posted

Apr 6, 2025

Last verified

Apr, 2025

Keywords

  • thrombosis
  • coagulopathy
  • influenza

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by University of Iowa on 2025-04-06.