Trials / Completed
CompletedNCT03553771
Safety and Efficacy of the LVIS and LVIS JR Devices in the Endovascular Treatment of Intracranial Aneurysms
A French, Multicenter, Prospective, Observational, "Real Life" Assessment of the Safety and Efficacy of the Low Profile Visualized Intraluminal Support (LVIS and LVIS JR) Devices in the Treatment of Intracranial Aneurysms
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 130 (actual)
- Sponsor
- Microvention-Terumo, Inc. · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
A French, multicenter, prospective, observational, "real life" assessment of the safety and efficacy of LVIS and LVIS JR devices in the treatment of intracranial aneurysms
Detailed description
This is a multicenter observational study. Treatment and follow-up visits will be done as per standard of care. The purpose of this study is to collect data on safety of the devices used since the French reimbursement. 130 patients will be enrolled over an 18-month recruitment period. All patients will be followed for at least 12 months.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | LVIS and LVIS JR | Braided coil assist stents used for aneurysm embolization |
Timeline
- Start date
- 2018-02-07
- Primary completion
- 2021-07-01
- Completion
- 2021-07-01
- First posted
- 2018-06-12
- Last updated
- 2024-01-24
Locations
20 sites across 1 country: France
Source: ClinicalTrials.gov record NCT03553771. Inclusion in this directory is not an endorsement.