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Effectiveness and Safety of Different Antithrombotic Therapy for the Treatment of Ventricular Thrombus

Effectiveness and Safety of Different Antithrombotic Therapy for the Treatment of Ventricular Thrombus

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05006677
Enrollment
480
Registered
2021-08-16
Start date
2021-08-04
Completion date
2023-12-30
Last updated
2023-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventricular Thrombus

Brief summary

To observe the effectiveness and safety of different therapies-non-vitamin K antagonist oral anticoagulants (NOACs) or vitamin K antagonists (VKAs) or antiplatelet agents and non-antithrombotic therapy - for the treatment of VT.

Interventions

DRUGnon-vitamin K antagonist oral anticoagulants (NOACs)

Collecting information of patients with VT who received NOACs

Collecting information of patients with VT who received VKAs

Collecting information of patients with VT who received antiplatelet agents

Collecting information of patients with VT without any antithrombotic therapy

Sponsors

China National Center for Cardiovascular Diseases
Lead SponsorOTHER_GOV

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults with ventricular thrombus(VT), regardless of sex, basic diseases, occupation or education; * The VT should be found newly within 3 months; * The observational phase should last until the time that patients who had achieved thrombus resolution. The following up period after the phase ended should continue for at least 3 months.

Exclusion criteria

* Individuals received standard antithrombotic therapy within 4 weeks; * Individuals received the thrombectomy therapy, ventricular aneurysm resection or heart transplantation within 6 weeks since the VT was found in the first time; * Had a long history of VT more than three months.

Design outcomes

Primary

MeasureTime frameDescription
Thrombus resolution in 12 weeks follow-up12 weeksThrombus resolution in 12 weeks follow-up

Secondary

MeasureTime frameDescription
Thrombus resolution in 6 months follow-up6 monthsThrombus resolution in 6 months follow-up
Thrombus resolution in 12 months follow-up12 monthsThrombus resolution in 12 months follow-up
Thrombus resolution in 6 weeks follow-up6 weeksThrombus resolution in 6 weeks follow-up
Bleeding12 monthsBleeding
All-cause death12 monthsAll-cause death
Thromboembolism events12 monthsThromboembolism events

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026