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NCT06462027 · ClinicalTrials.gov registry record · Phase 1

Packed Red Blood Cell Transfusion During Cardiac Arrest

A Phase 1 study of Cardiac Arrest, sponsored by NYU Langone Health.

Recruiting
Registry status
Phase 1
Development phase
30
Enrollment target
1
Study location

NCT06462027 is a Phase 1 study of Cardiac Arrest that is actively recruiting participants, run by NYU Langone Health. The registered enrollment target is 30 participants, below the 1,479-participant average among 31 other Cardiac Arrest trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06462027, a Phase 1 study of Cardiac Arrest, is actively recruiting participants, sponsored by NYU Langone Health.

RECRUITING
Registry status
Phase 1
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

The purpose of this pilot interventional study is to collect preliminary data on administering packed red blood cell (PRBC) during cardiac arrest (CA). The primary objective is to assess the feasibility of PRBC transfusion during cardiac CA to help optimize the methods required to augment cerebral and other vital organ oxygen delivery during cardiopulmonary resuscitation (CPR). The secondary objectives are to assess the effect of PRBC transfusion during prolonged cardiac arrests on cerebral oxygenation, end tidal carbon dioxide (ETCO2), return of spontaneous circulation (ROSC), survival to discharge, biomarkers of neural injury and inflammation, and neurological outcomes at hospital discharge, 30 days post-CA, and 90 days post-CA.

Conditions Studied

Interventions

  • OTHER Saline
  • DRUG Packed Red Blood Cells (1 unit)
  • DRUG Packed Red Blood Cells (2 units)

Study Locations (1)

New York

  • NYU Langone Health - New York

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2025-03-25
Est. Completion 2026-04-01
Phase Phase 1

Sponsor

NYU Langone Health

1,164 total trials

What the Registry Record Tells You About NCT06462027

The ClinicalTrials.gov registry entry for NCT06462027 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,479-participant average among 31 other Cardiac Arrest trials with a reported enrollment target (98% lower). The listed sponsor is NYU Langone Health, which has 1,164 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Cardiac Arrest appearing as the primary indexed condition, and to 3 interventions - of which Saline is the first listed.

NCT06462027 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT06462027 about?

NCT06462027 is a clinical study titled "Packed Red Blood Cell Transfusion During Cardiac Arrest". The purpose of this pilot interventional study is to collect preliminary data on administering packed red blood cell (PRBC) during cardiac arrest (CA). The primary objective is to assess the feasibility of PRBC transfusion during cardiac CA to help optimize the methods required to augment cerebral a...

What is the current status of trial NCT06462027?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2025-03-25. Estimated completion is 2026-04-01.

What conditions does trial NCT06462027 study?

This clinical trial studies the following conditions: Cardiac Arrest.

What interventions are being tested in trial NCT06462027?

The interventions under investigation include: Saline (OTHER), Packed Red Blood Cells (1 unit) (DRUG), Packed Red Blood Cells (2 units) (DRUG).

Who is sponsoring clinical trial NCT06462027?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06462027 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.