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ClotTriever Outcomes (CLOUT) Registry (CLOUT)

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ClinicalTrials.gov Identifier: NCT03575364
Recruitment Status : Active, not recruiting
First Posted : July 2, 2018
Last Update Posted : January 20, 2023
Information provided by (Responsible Party):
Inari Medical

Brief Summary:
Evaluate real world patient outcomes after treatment of acute, subacute, and chronic proximal lower extremity deep vein thrombosis (DVT) with the ClotTriever Thrombectomy System.

Condition or disease Intervention/treatment
Deep Vein Thrombosis Leg DVT Chronic DVT of Lower Extremity Acute DVT of Lower Extremity Device: ClotTriever

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Study Type : Observational [Patient Registry]
Actual Enrollment : 500 participants
Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration: 2 Years
Official Title: ClotTriever Outcomes (CLOUT) Registry
Actual Study Start Date : September 1, 2018
Actual Primary Completion Date : March 25, 2022
Estimated Study Completion Date : March 31, 2024

Group/Cohort Intervention/treatment
Primary Analytic
Patients with unilateral acute or subacute DVT of less than 6 weeks' duration.
Device: ClotTriever

Patients with proximal lower extremity DVT.
Device: ClotTriever

Primary Outcome Measures :
  1. Composite of Major Adverse Events (MAEs) [ Time Frame: 30 days ]
    All-cause mortality, major bleeding, symptomatic PE, or rethrombosis of target venous segment

Secondary Outcome Measures :
  1. Technical Success [ Time Frame: Index procedure ]
    Complete or near complete (75% or greater) removal of venous thrombus from the target venous segment

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with proximal lower extremity DVT.

Inclusion Criteria:

  • Proximal lower extremity DVT involving the femoral, common femoral, iliac veins, or inferior vena cava (IVC), alone or in combination.
  • Willing and able to provide informed consent.

Exclusion Criteria:

  • Prior venous stent in the target venous segment
  • IVC aplasia/hypoplasia or other congenital anatomic anomalies of the IVC or iliac veins
  • IVC filter in place at the time of the planned index procedure
  • Allergy, hypersensitivity, or thrombocytopenia from heparin or iodinated contrast agents, except for mild to moderate contrast allergies for which pretreatment can be used
  • Life expectancy less than 1 year
  • Chronic non-ambulatory status
  • Known hypercoagulable states that, in the opinion of the Investigator, cannot be medically-managed throughout the study period
  • Unavailability of a lower extremity venous access site

Information from the National Library of Medicine

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

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Sponsors and Collaborators
Inari Medical
Additional Information:

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Responsible Party: Inari Medical
ClinicalTrials.gov Identifier: NCT03575364    
Other Study ID Numbers: 18-001
First Posted: July 2, 2018    Key Record Dates
Last Update Posted: January 20, 2023
Last Verified: January 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Inari Medical:
Additional relevant MeSH terms:
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Venous Thrombosis
Embolism and Thrombosis
Vascular Diseases
Cardiovascular Diseases