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Ensayo clínico

Blood Purification for the Treatment of Pathogen Associated Shock

NCT: NCT05011656 · ACTIVE_NOT_RECRUITING

ID NCTNCT05011656
EstadoACTIVE_NOT_RECRUITING
Fecha de inicio2024-04-19
Finalización2027-07-31

Resumen breve

This study is a multi-center, randomized controlled feasibility trial to evaluate the initial safety and efficacy of a novel extracorporeal blood purification (EBP) therapy in critically ill patients with pathogen associated shock across 15 U.S. sites. Adults (18 years old and older) admitted to the ICU with all of the following: • Pathogen associated shock defined as: * The need for vasopressors to maintain mean arterial pressure (MAP) ≥ 65 mmHg despite adequate fluid resuscitation * Presence of a pathogen detected in the bloodstream within 72 hours of screening using commercially available in-vitro diagnostic testing

Fuente oficial

Ver en ClinicalTrials.gov →

Datos obtenidos de la API de ClinicalTrials.gov. Para conocer el estado más reciente, consulte el registro oficial.

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