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NCT05820451

Impella Real-World Surveillance of Patients Using Sodium Bicarbonate

Completed Last updated 4 September 2024
What this trial tests

trial testing Impella CP, 2.5, 5.0 and 5.5 with Sodium Bicarbonate used as purge solution in Cardiogenic Shock in 312 participants. Completed in 22 February 2024.

Timeline
15 December 2022
Primary endpoint
22 February 2024
22 February 2024

Quick facts

Lead sponsorAbiomed Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment312
Start date15 December 2022
Primary completion22 February 2024
Estimated completion22 February 2024
Sites20 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Abiomed Inc. — full company profile →

Who can join

Eligibility, any sex, with Cardiogenic Shock or High Risk PCI. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The population enrolled in this study are all subjects who received an Impella in which a bicarbonate-based purge solution was used.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Cardiogenic Shock

Currently open trials in the same condition.

Other Abiomed Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05820451.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing