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SUSPENDED
NCT06462027
PHASE1

Packed Red Blood Cell Transfusion During Cardiac Arrest

Sponsor: NYU Langone Health

View on ClinicalTrials.gov

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.

Official title: A Single-center, Randomized, Placebo Controlled Pilot Study of Packed Red Blood Cell Transfusion During Prolonged Adult In-hospital Cardiac Arrest

Key Details

Gender

All

Age Range

18 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-06-01

Completion Date

2027-09-01

Last Updated

2026-04-09

Healthy Volunteers

No

Conditions

Interventions

DRUG

Packed Red Blood Cells (1 unit)

500 mL of packed red blood cells administered intravenously 10-20 minutes after CA onset, provided Return of Spontaneous Circulation (ROSC) has not been achieved.

DRUG

Packed Red Blood Cells (2 units)

1000 mL of packed red blood cells administered intravenously 10-20 minutes after CA onset, provided Return of Spontaneous Circulation (ROSC) has not been achieved.

OTHER

Saline

Control subjects will receive 500mL of normal saline intravenously.

Locations (1)

NYU Langone Health

New York, New York, United States