Actively Recruiting

All Genders
ID06871683

ClotTriever4 Thrombectomy System Use-Result Survey in Japan

Led by Inari Medical · Updated on 2026-05-27

100

Participants Needed

13

Research Sites

39 weeks

Total Duration

On this page

Sponsors

I

Inari Medical

Lead Sponsor

V

Vorpal Technologies

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are observing the use of the ClotTriever4 Thrombectomy System in treating patients with deep vein thrombosis who have acute severe symptoms. The study aims to assess the safety and effectiveness of this device during everyday clinical practice after it was approved for marketing in Japan. This survey is important as it evaluates real-world results following regulatory approval. Participants will receive treatment using the ClotTriever4 Thrombectomy System, which is designed to remove blood clots from veins. The survey includes all patients in Japan who have the device inserted into their blood vessels as part of their treatment. There are no separate treatment groups; everyone treated with the device is included. During the study, researchers will monitor participants for any major adverse events up to 30 days after the procedure. They will also assess whether the device successfully completes the clot removal during the procedure itself. The survey will continue until December 2028 and collects data from all treated patients to understand the device's performance in general clinical use.

CONDITIONS

Brief Title

ClotTriever® Thrombectomy System Use-Result Survey in Japan

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients treated with the ClotTriever4 Thrombectomy System in Japan
  • Diagnosis of deep vein thrombosis with acute severe symptoms
  • No age or gender restrictions
  • Willingness to have treatment data included in the survey
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Day of the procedure

Participants undergo treatment using the ClotTriever® Thrombectomy System for deep vein thrombosis with acute severe symptoms.

1 visit (in-person)

Post-operative Follow-up

Duration - 30 days post procedure

Participants are monitored for major adverse events and treatment success after the thrombectomy procedure.

Follow-up visits during the 30 days post procedure

Trial Site Locations

Total: 13 locations

1

Chiba University Hospital

Chuo, Chiba, Japan, 260-8677

Enrolling by Invitation

2

Ota Memorial Hospital

Ōta, Gunma, Japan, 373-8585

Enrolling by Invitation

3

St. Marianna University Hospital

Kawasaki, Kanagawa, Japan, 216-8511

Enrolling by Invitation

4

National Cerebral and Cardiovascular Center

Suita, Osaka, Japan, 564-8565

Enrolling by Invitation

5

Asahikawa Medical Hospital

Asahikawa, Japan, 078-8510

Actively Recruiting

6

Asahi General Hospital

Chiba, Japan, 289-2511

Actively Recruiting

7

Nozaki Tokushukai Hospital

Daitō, Japan, 574-0074

Actively Recruiting

8

Shonan Kamakura

Kanagawa, Japan, 247-8533

Actively Recruiting

9

Kyoto Katsura Hospital

Kyoto, Japan, 615-8256

Enrolling by Invitation

10

Nara City Hospital

Nara, Japan, 630-8305

Actively Recruiting

11

Osaka Police Hospital

Osaka, Japan, 543-0042

Actively Recruiting

12

Mitsui Memorial Hospital

Tokyo, Japan, 101-8643

Actively Recruiting

13

Mie University

Tsu, Japan, 514-0102

Actively Recruiting

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Research Team

S

Satoko Inoue

A

Anthony Vogt

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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