- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Sleep disturbances (incl subtypes).
Displaying page 1 of 1.
| EudraCT Number: 2013-001832-23 | Sponsor Protocol Number: NEU_CH_7911 | Start Date*: 2013-10-23 | |||||||||||
| Sponsor Name:Neurim Pharmaceuticals (1991) Ltd. | |||||||||||||
| Full Title: A RANDOMIZED, PLACEBO-CONTROLLED STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF CIRCADIN® TO ALLEVIATE SLEEP DISTURBANCES IN CHILDREN WITH NEURODEVELOPMENTAL DISABILITIES | |||||||||||||
| Medical condition: SLEEP DISTURBANCES IN CHILDREN WITH NEURODEVELOPMENTAL DISABILITIES | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA FI (Completed) GB (Completed) NL (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002116-32 | Sponsor Protocol Number: MTM-04 | Start Date*: 2015-09-23 | ||||||||||||||||||||||||||
| Sponsor Name:Køge Hospital | ||||||||||||||||||||||||||||
| Full Title: The effect of MElatonin on Depression, Anxiety, CIrcadian and Sleep disturbances in patients after acute myocardial syndrome | ||||||||||||||||||||||||||||
| Medical condition: Depression Anxiety Sleep disturbances Circadian disturbances | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2010-022460-12 | Sponsor Protocol Number: MVH-03 | Start Date*: 2011-03-23 | ||||||||||||||||||||||||||
| Sponsor Name:Herlev Hospital | ||||||||||||||||||||||||||||
| Full Title: The effect of melatonin on depression, anxiety, cogntive function and sleep disturbances in breast cancer patients | ||||||||||||||||||||||||||||
| Medical condition: Depression Anxiety Postoperative cognitive dysfunction Sleep disturbances | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2004-002505-74 | Sponsor Protocol Number: CEP1538/3034/ES/MN | Start Date*: 2005-01-05 | |||||||||||
| Sponsor Name:Cephalon Europe, A Division of Cephalon UK Limited | |||||||||||||
| Full Title: A 6 month open-label, flexible-dosage study to assess the safety and effectiveness of PROVIGIL® (Modafinil) treatment in children and adolescents with excessive sleepiness associated with narcoleps... | |||||||||||||
| Medical condition: Excessive sleepiness associated with Narcolepsy or Obstructive Sleep Apnea/Hypopnea Syndrome. | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) FI (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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Query did not match any studies.