Last reviewed · How we verify

NCT05208398

Apixaban in Patients With Left Ventricular Thrombus

Completed Phase 3 Last updated 26 January 2022
What this trial tests

Phase 3 trial testing Apixaban in Left Ventricular Thrombus in 50 participants. Completed in 30 September 2021.

Timeline
18 February 2018
Primary endpoint
30 September 2021
30 September 2021

Quick facts

Lead sponsorSaud Al Babtain Cardiac Center
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment50
Start date18 February 2018
Primary completion30 September 2021
Estimated completion30 September 2021
Sites1 location across Saudi Arabia

Drugs / interventions tested

Conditions studied

Sponsor

Saud Al Babtain Cardiac Center

Who can join

Adults 18 to 80, any sex, with Left Ventricular Thrombus. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Open label randomized controlled clinical trial to evaluate the efficacy and safety of apixaban versus warfarin in treating left ventricular thrombus in patients with acute or recent myocardial infarction (MI).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Apixaban in Patients With Post-Myocardial Infarction Left Ventricular Thrombus: A Randomized Clinical Trial.
    Youssef AA, Alrefae MA, Khalil HH, Abdullah HI, et al · · 2023 · cited 24× · PMID 37013071 · DOI 10.1016/j.cjco.2022.12.003

Verify or expand the search:

Other trials of Apixaban

Trials testing the same drug.

Other recruiting trials for Left Ventricular Thrombus

Currently open trials in the same condition.

Other Saud Al Babtain Cardiac Center 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/NCT05208398.

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