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COVID plasma trial pulled before it even started

NCT ID NCT04411602

Disease control Sponsor: Henry Ford Health System Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled This study
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study planned to give blood plasma from recovered COVID-19 patients to people in the ICU with severe COVID-19. The goal was to see if it could help them breathe better and survive. However, the trial was withdrawn before enrolling any participants, so no results are available.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Started

Apr 2020

Finished

Apr 2021

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Laboratory confirmed COVID-19 * Severe or Immediately life threatening COVID-19 * Dyspnea * Respiratory frequency \> 30/minute * Blood oxygen saturation \<93% * Life-threatening disease is defined as the following * Respiratory Failure. * Septic shock, and/or, * Multiple organ dysfunction or failure. Exclusion Criteria: * Contraindication to transfusion (severe volume overload, history of anaphylaxis to blood products). * Other documented uncontrolled infection. * Severe DIC needing factor replacement, FFP, cryoprecipitate. * On dialysis. * Active intracranial bleeding. * Clinically significant myocardial ischemia.

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Conditions

The condition(s) this trial relates to.

COVID-19 severe acute respiratory syndrome

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

COVID Severe acute respiratory syndrome

Contacts and locations

Locations

  • Ascension Macomb-Oakland Hospital, Warren Campus

    Warren, Michigan, 48093, United States

  • Ascension Providence Hospital, Novi Campus

    Novi, Michigan, 48374, United States

  • Ascension Providence Hospital, Southfield Campus

    Southfield, Michigan, 48075, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.