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Evaluation of the Valiant Captivia Physician Fenestrated Stent Graft System in Aortic Arch and Descending Thoracic Aorta Pathologies

Study acronym: EVERGREEN
StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated May 1, 2024 (before its estimated November 2024 completion). Its status may not reflect the trial's current state.

Record History

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  1. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 4
    • Start date changed from estimate of Oct 2023 to Nov 21, 2023
    • Eligibility criteria expanded, about 63 words
    v4
  2. Primary completion date: Dec 2023 to Nov 2024v3 Show 4 more changesShow less
    • Start date: Mar 2023 to Oct 2023
    • Study completion date: Nov 2026 to Oct 2027
    • Eligibility criteria revised
    • Study title shortened, about 1 word
  3. Start date: Nov 2022 to Mar 2023
    • Secondary endpoints revised (12)
    v2
  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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Ceric Sàrl
10 trials monitored
See 1 trial at risk
The study objectives are to assess safety and effectiveness, measured acutely and at the 30-day visit after implantation of the Valiant Captivia physician fenestrated Stent Graft. Clinical utility measures throughout the procedure and until discharge will be assessed
Trial Details
NCT Number NCT05479305
Lead Sponsor Ceric Sàrl
Collaborators: European Cardiovascular Research Center
Conditions
(from sponsor)		 Penetrating Ulcer of Aorta, Aneurysm Aortic, Type B Aortic Dissection, Residual Dissection After Type A Repair
Related terms Aortic Aneurysm
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov