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Safety and Effectiveness of Mechanical Thrombectomy Using the Anaconda ANA Funnel Catheter

Study acronym: ATHENA
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Primary completion date: Feb 2027 to Aug 2027 Completion date: May 2027 to Dec 2027 · Eligibility criteria expanded, about 14 words · Study title expanded, about 1 wordv4 Show 3 more changesShow less
    • Completion date: May 2027 to Dec 2027
    • Eligibility criteria expanded, about 14 words
    • Study title expanded, about 1 word

    See this version in full on ClinicalTrials.gov ↗

  2. Primary completion date: Dec 2025 to Feb 2027 Primary endpoints revised (2) · Enrollment target: 250 to 327 · Study sites: 1 to 22 · 3 morev3 Show 6 more changesShow less
    • Primary endpoints revised (2)
    • Enrollment target: 250 to 327
    • Study sites: 1 to 22
    • Completion date: Mar 2026 to May 2027
    • Eligibility criteria expanded, about 144 words
    • Study description shortened, about 160 words

    See this version in full on ClinicalTrials.gov ↗

  3. Trial status: Not Yet Recruiting to Recruiting Study sites: 0 to 1 · Start date changed from estimate of Sep 2024 to Sep 9, 2024 · Eligibility criteria expanded, about 6 wordsv2 Show 3 more changesShow less
    • Study sites: 0 to 1
    • Start date changed from estimate of Sep 2024 to Sep 9, 2024
    • Eligibility criteria expanded, about 6 words

    See this version in full on ClinicalTrials.gov ↗

  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 objective of this study is to assess the safety and effectiveness of mechanical thrombectomy (MT) using the ANA funnel catheter in its intended use, which is to facilitate the navigation and deployment of other neurovascular devices and to allow flow arrest during mechanical thrombectomy procedures performed in subjects experiencing acute ischemic stroke (AIS) secondary to large vessel occlusion (LVO) and treated within 24 hours of symptom onset.
Trial Details
NCT Number NCT06370182
Lead Sponsor Anaconda Biomed S.L.
Conditions Acute Ischemic Stroke From Large Vessel Occlusion
Enrollment 327 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov