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Brain State-dependent PCMS in Chronic Stroke

StatusNot Yet Recruiting
PhasePhase 1/2
Started
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Record History

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  1. Re-verified, no change to tracked fieldsv7
  2. Primary completion date: Jul 2024 to Jul 2030v6 Show 4 more changesShow less
    • Start date: Jun 1, 2022 to Jan 1, 2026
    • Trial status: Recruiting to Not Yet Recruiting
    • Study completion date: Jul 2025 to Jul 2031
    • Site details revised
  3. Re-verified, no change to tracked fieldsv5
  4. Start date changed from estimate of Jun 2022 to Jun 1, 2022v4
  5. Interventions: Phase-dependent paired corticomotoneuronal stimulation (PCMS) (Combination Product) to Brain state-dependent paired corticomotoneuronal stimulation (PCMS) (Combination Product)
    • Secondary endpoints: 1 to 2
    • Eligibility criteria expanded, about 2 words
    • Study title expanded, about 1 word
    v3
  6. Trial status: Not Yet Recruiting to Recruiting
    • Start date: Jul 2021 to Jun 2022
    • Site details revised
    v2
  7. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
After stroke, people often have difficulty using their hands. Combined brain and nerve stimulation can strengthen the neural pathways that control hand function. In this study, we will deliver combined brain and nerve stimulation during specific time windows that increase activation of neural pathways underlying hand function. We will compare the effects of combined brain and nerve stimulation during these optimal time windows to the effects of combined brain and nerve stimulation applied during random time windows on post-stroke hand function.
Trial Details
NCT Number NCT04830163
Lead Sponsor University of Texas at Austin
Conditions
(from sponsor)		 Stroke
Related terms Bronchiolitis Obliterans Syndrome, Stroke
Enrollment 45 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov