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Treating Young Children With Attention Deficit Hyperactivity Disorder

Study acronym: TYCA
StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Recruitment opened Start date changed from estimate of Feb 2026 to Feb 16, 2026 · Site details revised at 5 of 5 sitesv3 Show 2 more changesShow less
    • Start date changed from estimate of Feb 2026 to Feb 16, 2026
    • Site details revised at 5 of 5 sites
  2. Notable Primary endpoint revised Secondary endpoints: details revised at 7 of 7 entriesv2 Show 1 more changeShow less
    • Secondary endpoints: details revised at 7 of 7 entries

    See this version in full on ClinicalTrials.gov ↗

  3. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This project will evaluate the effectiveness of Methylphenidate versus Guanfacine in treating Attention-Deficit/Hyperactivity Disorder (ADHD) in children aged 3 through 5 years (inclusive), as measured by clinician rating of global improvement.
Trial Details
NCT Number NCT07300956
Lead Sponsor Children's Hospital Medical Center, Cincinnati
Collaborators: Patient-Centered Outcomes Research Institute, Children's Hospital of Philadelphia, Developmental Behavioral Pediatrics Research Network, Boston Children's Hospital, Boston, MA, USA, Children's Mercy Hospital Kansas City, Stanford University
Conditions Attention-Deficit/Hyperactivity Disorder (ADHD)
Enrollment 370 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov