Trials / Not Yet Recruiting
Not Yet RecruitingNCT06893588
Registry on NeVa VS for CerebraL VAsospasm ManagemenT in Post SAH PatiEnts
Prospective, Open-Label, Multi-Center ProceDural Data CollectIon Case Registry on NeVa VS for CerebraL VAsospasm ManagemenT in Post SAH PatiEnts (The DILATE Registry)
- Status
- Not Yet Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 200 (estimated)
- Sponsor
- Vesalio · Industry
- Sex
- All
- Age
- 22 Years
- Healthy volunteers
- Not accepted
Summary
A multi-center, observational registry study intended to assess the HDE-approved NeVa VS cerebral artery dilation device in patients with symptomatic cerebral vasospasm caused by aneurysmal subarachnoid hemorrhage (aSAH)
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | NEVA VS | cerebral artery dilation device |
Timeline
- Start date
- 2025-04-14
- Primary completion
- 2027-02-14
- Completion
- 2027-03-15
- First posted
- 2025-03-25
- Last updated
- 2025-03-25
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06893588. Inclusion in this directory is not an endorsement.