ClotTriever Outcomes (CLOUT) Registry (CLOUT)
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|ClinicalTrials.gov Identifier: NCT03575364|
Recruitment Status : Enrolling by invitation
First Posted : July 2, 2018
Last Update Posted : December 17, 2021
|Condition or disease||Intervention/treatment|
|Deep Vein Thrombosis Leg DVT Chronic DVT of Lower Extremity Acute DVT of Lower Extremity||Device: ClotTriever|
|Study Type :||Observational [Patient Registry]|
|Estimated Enrollment :||500 participants|
|Target Follow-Up Duration:||2 Years|
|Official Title:||ClotTriever Outcomes (CLOUT) Registry|
|Actual Study Start Date :||September 1, 2018|
|Estimated Primary Completion Date :||March 31, 2022|
|Estimated Study Completion Date :||March 31, 2024|
Patients with unilateral acute or subacute DVT of less than 6 weeks' duration.
Patients with proximal lower extremity DVT.
- Composite of Major Adverse Events (MAEs) [ Time Frame: 30 days ]All-cause mortality, major bleeding, symptomatic PE, or rethrombosis of target venous segment
- Technical Success [ Time Frame: Index procedure ]Complete or near complete (75% or greater) removal of venous thrombus from the target venous segment
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03575364