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Bipolinis sutrikimas klinikiniai tyrimai Ohio
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Oficialus tyrimo tekstas (anglų kalba)
Safety and Tolerability Trial of Lumateperone in Pediatric Patients With Schizophrenia, Bipolar Disorder or Autism Spectrum Disorder
- University of Cincinnati Medical Center, Cincinnati
- Charak Center for Health and Wellness, Garfield Heights
Renkami dalyviai3 fazė
Amžius nuo 5 iki 17 · Visoms lytims · Atnaujinta 2026-09-25 · NCT06229210Multicenter Study of Lumateperone for the Treatment of Bipolar Depression in Pediatric Patients
- University of Cincinnati Medical Center, Cincinnati
- Charak Center for Health and Wellness, Garfield Heights
Renkami dalyviai3 fazė
Amžius nuo 10 iki 17 · Visoms lytims · Atnaujinta 2026-09-25 · NCT06372964A Study to Evaluate the Effectiveness of Valbenazine in Adult Participants With Tardive Dyskinesia (TD) Who Remain Symptomatic While Receiving or After Stopping a Vesicular Monoamine Transporter 2 (VMAT2) Inhibitor
- Neurocrine Clinical Site, Independence
Renkami dalyviai4 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-18 · NCT07105111A Study to Assess Adverse Events and Change in Disease Activity of Oral Icalcaprant in Adult Participants With Bipolar I or II Disorder
- University Of Cincinnati Medical Center /ID# 274160, Cincinnati
- The Ohio State University /ID# 272954, Columbus
Renkami dalyviai2 fazė
Amžius nuo 18 iki 65 · Visoms lytims · Atnaujinta 2026-08-14 · NCT06696755Child Bipolar Network Ketogenic Diet Approach to Bipolar Disorder in Adolescents
- University of Cincinnati College of Medicine, Cincinnati
Renkami dalyviaiNurodytas atlygis dalyviams
Amžius nuo 12 iki 21 · Visoms lytims · Atnaujinta 2026-04-22 · NCT06920940Attentional Biases, Reward Sensitivity, and Cognitive Control in Adults With Bipolar Disorder
- University Hospitals Cleveland Medical Center - Mood Disorders Program, Cleveland
Renkami dalyviaiStebimasis tyrimasLaukiami sveiki savanoriai
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2025-10-10 · NCT03829787Iš ClinicalTrials.gov, duomenys gauti 2026-10-04. Kiekvienas tyrimas nustato savo tinkamumo kriterijus; tyrimo komanda sprendžia, kas gali dalyvauti.