ClotTriever® Thrombectomy System Use-Result Survey in Japan
Condition(s) studied
Investigational drug(s) / intervention(s)
ClotTriever® Thrombectomy System: ClotTriever® Thrombectomy System use for treatment of patients with deep vein thrombosis with acute severe symptoms.
Study summary
The objective of this survey is to determine the safety and efficacy of the ClotTriever Thrombectomy System under daily clinical practice after marketing approval in Japan.
This device was designated as a subject of use results evaluation at the time of application for manufacturing and marketing approval.
Eligibility
Primary outcome measure(s)
- Rate of Major Adverse Events — Through 30 days post index procedure.
Rate of Major Adverse Events \[All-cause mortality, Major bleeding, New symptomatic Pulmonary Embolism (PE) documented by Computed Tomography Pulmonary Angiography (CTPA), Rethrombosis of a Target Venous Segment\]. - Technical Success — During the index procedure
Thrombus residual volume assessed by the the treating physician using pre- and post-procedure venography to evaluate the success of thrombus removal.
Trial sites (15)
| Facility | City | Region | Status |
|---|---|---|---|
| Chiba University Hospital | Chuo | Chiba | |
| Ota Memorial Hospital | Ōta | Gunma | |
| St. Marianna University Hospital | Kawasaki | Kanagawa | |
| National Cerebral and Cardiovascular Center | Suita | Osaka | |
| Asahikawa Medical Hospital | Asahikawa | Japan | |
| Asahi General Hospital | Chiba | Japan | |
| Nozaki Tokushukai Hospital | Daitō | Japan | |
| Shonan Kamakura | Kanagawa | Japan | |
| Kyoto Katsura Hospital | Kyoto | Japan | |
| Nara City Hospital | Nara | Japan | |
| Osaka Police Hospital | Osaka | Japan | |
| Mitsui Memorial Hospital | Tokyo | Japan | |
| Keio University | Tokyo | Japan | |
| Teikyo University | Tokyo | Japan | |
| Mie University | Tsu | Japan |
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06871683 on ClinicalTrials.gov ↗ ← All trials in Japan