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Personalized Therapy Study - HFRS (TriageHF) Post Approval Study

StatusActive, Not Recruiting
PhaseNot specified
SponsorMedtronic
Started
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Record History

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  1. Minor Primary completion date changed from estimate of May 12, 2025 to Dec 6, 2024
    • Study completion date: Jan 31, 2027 to Jan 31, 2028
    v19
  2. Minor Primary completion date: Jan 31, 2025 to May 12, 2025
    • Study sites revised (92)
    v18
  3. Minor Trial status: Recruiting to Active, Not Recruiting
    • Study sites: 113 to 92
    v17
  4. Minor Study sites: 114 to 113v16
  5. Minor Site details revised at 1 of 114 sitesv15
Show 13 earlier versionsHide 13 earlier versions
  1. Minor Site details revised at 1 of 114 sitesv14
  2. Minor Site details revised at 1 of 114 sitesv13
  3. Minor Site details revised at 1 of 114 sitesv12
  4. Minor Site details revised at 4 of 114 sitesv11
  5. Minor Study sites: 115 to 114v10
  6. Minor Study sites: 109 to 115v9
  7. Minor Study sites: 87 to 109v8
  8. Minor Study sites: 61 to 87v7
  9. Minor Study sites: 52 to 61v6
  10. Minor Study sites: 47 to 52v5
  11. Minor Study sites: 44 to 47v4
  12. Minor Study sites: 38 to 44v3
  13. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 33 to 38
    v2
  1. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
16 trials monitored
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8,786 trials monitored
See 412 trials at risk
1,995 trials monitored
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Medtronic is sponsoring the HFRS PAS to evaluate the HFRS feature (TriageHF) when used in routine clinical practice following commercial release. The HFRS PAS is conducted within Medtronic's Product Surveillance Registry (PSR) platform.
Trial Details
NCT Number NCT04489225
Lead Sponsor Medtronic
Conditions
(from sponsor)
Heart Failure
Related terms Heart Failure
Enrollment 2,200 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov