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Microvention AnEurysm & STroke Real-life Data cOllection

Study acronym: MAESTRO
StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Primary endpoints: 1 to 2v5 Show 5 more changesShow less
    • Enrollment target: 750 to 1000
    • Interventions: All Microvention Class III implantable device CE marked (Device) to All Microvention Class III implantable device CE marked (Device), All Microvention Mechanical Thrombectomy Class III device CE marked…
    • Eligibility criteria expanded, about 97 words
    • Study arms: 0 to 2
    • Study description expanded, about 3 words
  2. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Primary completion date: Dec 31, 2029 to Dec 30, 2029
    • Start date changed from estimate of Oct 30, 2024 to Dec 30, 2024
    v4
  3. Primary endpoint revisedv3
  4. Primary endpoint revisedv2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The MAESTRO registry is a post-market, single-arm, non-interventional, multicenter registry
Trial Details
NCT Number NCT06494436
Lead Sponsor Microvention-Terumo, Inc.
Conditions
(from sponsor)		 Intracranial Aneurysm, Intracranial Aneurysm, Wide Neck Aneurysm, Large Neck Aneurysm Lesion, Aneurysmal Subarachnoid Hemorrhage, Ischemic Stroke, Acute Ischemic Stroke
Related terms Intracranial Aneurysm, Ischemic Stroke, Subarachnoid Hemorrhage
Enrollment 1,000 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov