- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Delayed sleep phase syndrome.
Displaying page 1 of 1.
| EudraCT Number: 2007-005986-36 | Sponsor Protocol Number: 7977 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:University of Bergen | |||||||||||||
| Full Title: DELAYED SLEEP PHASE SYNDROME. SLEEP, PERSONALITY, DEVELOPMENTAL HISTORY, CIRCADIAN RHYTHM AND TREATMENT | |||||||||||||
| Medical condition: Delayed sleep phase syndrome - DSPS. | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000220-18 | Sponsor Protocol Number: C.2524.0472.01 | Start Date*: 2013-03-25 |
| Sponsor Name:University of Amsterdam | ||
| Full Title: Effects of melatonin treatment, light therapy, and sleep improvement on psychosocial, cognitive, and behavioural outcomes in children with Delayed Sleep Phase Syndrome and their parents | ||
| Medical condition: Delayed Sleep Phase Syndrome | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000320-18 | Sponsor Protocol Number: FASE01 | Start Date*: 2012-11-22 | ||||||||||||||||
| Sponsor Name:Parnassia Bavo Groep - PsyQ | ||||||||||||||||||
| Full Title: Phase shift in adult ADHD of sleep and apetite. | ||||||||||||||||||
| Medical condition: Delayed Sleep Phase Syndrome (DSPS) in adult patients with Attention-Deficit/Hyperctivity Disorder (ADHD) | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-000821-29 | Sponsor Protocol Number: SPD503-401 | Start Date*: 2020-11-19 | |||||||||||
| Sponsor Name:Takeda Development Center Americas, Inc. | |||||||||||||
| Full Title: A Phase 4, Multicenter, 2-part Study Composed of a 1-Year Randomized, Double-blind, Parallel-group, Placebo-controlled, Active-comparator, Dose-optimization Evaluation followed by a 1-Year Open-lab... | |||||||||||||
| Medical condition: Attention-deficit/hyperactivity disorder (ADHD) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) NL (Trial now transitioned) SE (Trial now transitioned) AT (Prematurely Ended) ES (Ongoing) BE (Trial now transitioned) PT (Prematurely Ended) GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-006067-28 | Sponsor Protocol Number: CST103/CST107-CLIN-011 | Start Date*: 2022-01-10 | ||||||||||||||||||||||||||
| Sponsor Name:CuraSen Therapeutics, Inc. | ||||||||||||||||||||||||||||
| Full Title: A Phase II, Randomized, Placebo-Controlled, Double-Blind, Crossover, Study of the Pharmacodynamic Effects of CST-103 co-administered with CST-107 on the Central Nervous System in Subjects with Neur... | ||||||||||||||||||||||||||||
| Medical condition: Patients with Parkinson’s Disease with REM sleep behaviour disorder, Mild Cognitive Impairment, Dementia with Lewy Bodies and Parkinson’s Disease Dementia. | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
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Query did not match any studies.