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A Neuromodulation Auditory System to Optimize Patient Experience During Dysfunctional Dialysis Access Endovascular Procedures

StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Trial completed Show 4 more changesShow less
    • Study completion date changed from estimate of Mar 30, 2026 to Jan 1, 2026
    • Primary completion date: Dec 30, 2025 to Jan 1, 2026
    • Eligibility criteria expanded, about 8 words
    • Site details revised at 1 of 2 sites
  2. Re-verified, no change to tracked fieldsv2
  3. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Peri-procedural stress is a common challenge in interventional radiology that can negatively impact patient tolerance and the overall procedural experience. This randomized controlled trial (RCT) was designed to evaluate the clinical impact of a non-commercially available, newly-developed structured auditory neuromodulation system, designed to optimize patient experience during endovascular procedures for dysfunctional dialysis access.
Trial Details
NCT Number NCT07467642
Lead Sponsor Attikon Hospital
Conditions
(from sponsor)		 Dialysis Access Dysfunction, Endovascular Procedure, Patient Experience, Neuromodulation
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov