Xenon for Neuroprotection During Post-Cardiac Arrest Syndrome in Comatose Survivors of an Out of Hospital Cardiac Arrest

PHASE3Not yet recruitingINTERVENTIONAL
Enrollment

1,436

Participants

Timeline

Start Date

March 31, 2026

Primary Completion Date

April 30, 2029

Study Completion Date

May 31, 2030

Conditions
Post-Cardiac Arrest Syndrome
Interventions
COMBINATION_PRODUCT

Xenon

50% xenon by inhalation, delivered by customized xenon delivery system, that includes a ventilator, for the 24h period of TH/TTM. The inhalation therapy is provided in combination with protocol-directed Post-Cardiac Arrest Care dictated by the 2015 guidelines from the American Heart Association and the European Resuscitation Council.

Trial Locations (10)

14203

University at Buffalo, Buffalo

32611

University of Florida, Gainesville

38120

Baptist Memorial Hospital, Baptist Clinical Research Institute, Memphis

39503

Memorial Hospital at Gulfport, Gulfport

43210

Wexner Medical Center, Ohio State University, Columbus

68198

University Nebraska Medical Center, Omaha

77030

Houston Methodist Research Institute, Houston

06102

Hartford Hospital, Hartford

Unknown

Aalborg University Hospital, Aalborg

University Hospital, Rigshospitalet, Blegdamsvej 9, Copenhagen

Sponsors
All Listed Sponsors
lead

Invero Pharma, Inc.

INDUSTRY