- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: EEC syndrome.
Displaying page 1 of 1.
| EudraCT Number: 2013-005017-12 | Sponsor Protocol Number: EyeADHD-01 | Start Date*: 2014-03-31 | |||||||||||
| Sponsor Name:Parnassia Bavo Groep - PsyQ | |||||||||||||
| Full Title: Looking into the eye of ADHD. Investigating the relationship between ADHD, the delayed circadian rhythm and the functioning of the eye. | |||||||||||||
| Medical condition: Adults with ADHD and suboptimal eye functioning. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001689-97 | Sponsor Protocol Number: LOC/07-11 | Start Date*: 2009-12-11 | |||||||||||
| Sponsor Name:CHU de Rennes | |||||||||||||
| Full Title: Etude de la relation dose-effet de la mélatonine dans l'autisme infantile. | |||||||||||||
| Medical condition: Autisme infantile, notamment les troubles du sommeil et de la communication | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2020-001530-35 | Sponsor Protocol Number: MeCOVID | Start Date*: 2020-04-09 |
| Sponsor Name:Fundación para la Investigación Biomédica del Hospital La Paz (FIBHULP) | ||
| Full Title: Randomized multicenter clinical trial to evaluate the efficacy of melatonin in the prophylaxis of SARS-CoV-2 infection in high-risk contacts. COVID-19 | ||
| Medical condition: SARS-CoV-2 infection in high-risk contacts | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-002697-37 | Sponsor Protocol Number: 14/0382 | Start Date*: 2015-04-15 | ||||||||||||||||
| Sponsor Name:University College London | ||||||||||||||||||
| Full Title: Single-centre open label exploratory phase IIb pilot study of exogenous oral Melatonin for the treatment of Nocturia in adults with Parkinson’s disease | ||||||||||||||||||
| Medical condition: Parkinson's Disease Nocturia | ||||||||||||||||||
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| Population Age: | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-001960-31 | Sponsor Protocol Number: S54348 | Start Date*: 2013-05-03 |
| Sponsor Name:UZ Leuven | ||
| Full Title: Combined drug Approach to Prevent Ischemia-reperfusion injury during Transplantation of Livers (CAPITL): a first-in-men study | ||
| Medical condition: Investigation of the ischemia-reperfusion injury in patients who will undergo a liver transplantation after receiving a drug combination/multifactorial modulation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
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