- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Pointing.
Displaying page 1 of 1.
EudraCT Number: 2005-003903-35 | Sponsor Protocol Number: : NUTH-2005-03384 | Start Date*: 2006-01-19 |
Sponsor Name:Newcastle-upon-Tyne Hospitals NHS Trust | ||
Full Title: : The Role of Keppra in the Treatment of Tremor in Multiple Sclerosis | ||
Medical condition: Multiple Sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000494-67 | Sponsor Protocol Number: 1.2 | Start Date*: 2013-10-22 | |||||||||||
Sponsor Name:Klinik for håndkirurgi, Gentofte hospital | |||||||||||||
Full Title: Needle fasciotomi vs collagenase for treatment of Dupuytrens contracture in 2nd, 3rd, 4th and 5th metacarpophalangeal joint. | |||||||||||||
Medical condition: Dupuytrens contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003784-30 | Sponsor Protocol Number: CHUBX2011/20 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHU de bordeaux | |||||||||||||
Full Title: Rubinstein-Taybi syndrome: approach to functional imaging and therapeutic trial | |||||||||||||
Medical condition: Rubinstein-Taybi Syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000048-32 | Sponsor Protocol Number: 15-062 | Start Date*: 2018-03-01 |
Sponsor Name:RWTH Aachen University/CTC-A | ||
Full Title: Evaluation of the Therapeutic Effects of Testosterone on Pain Perception in case of Chronic Pain Disorder | ||
Medical condition: Patient with persistent somatoform pain disorder (F45.40 or F45.41) should be included into the study. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-000222-19 | Sponsor Protocol Number: H2020-PHC-18-2015-667224 | Start Date*: 2017-08-02 | ||||||||||||||||
Sponsor Name:University Hospital Tuebingen | ||||||||||||||||||
Full Title: Effect of ALlopurinol in addition to hypothermia for hypoxic-ischemic Brain Injury on Neurocognitive Outcome – a blinded randomized placebo-controlled parallel group multicenter trial for superiori... | ||||||||||||||||||
Medical condition: Perinatal Asphyxia, hypoxic-ischemic brain injury | ||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) NO (Trial now transitioned) ES (Ongoing) FI (Trial now transitioned) EE (Trial now transitioned) AT (Trial now transitioned) BE (Trial now transitioned) PT (Prematurely Ended) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
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