- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Triceps.
Displaying page 1 of 1.
EudraCT Number: 2004-004215-35 | Sponsor Protocol Number: TENPET | Start Date*: 2005-01-19 |
Sponsor Name:Turku PET Centre | ||
Full Title: Influence of muscle specific activation on regional glucose uptake in the human Achilles tendon | ||
Medical condition: The combined forces generated by the triceps surae muscles causes non-uniform strain within the human triceps aponeuroses. This may cause non-uniform tendon force that would result in intratendinou... | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004474-42 | Sponsor Protocol Number: V3_06082015 | Start Date*: 2015-05-07 | |||||||||||
Sponsor Name:Copenhagen University Hospital at Hvidovre | |||||||||||||
Full Title: Treatment of equinus gait caused by dynamic tightening of the calf muscles in children with cerebral palsy. A randomized, placebo controlled Botulinum toxin type A volume/response study. | |||||||||||||
Medical condition: Treatment of equinus gait caused by dynamic tightening of the calf muscles in children with cerebral palsy. | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000901-35 | Sponsor Protocol Number: 2016-02 | Start Date*: 2017-07-10 |
Sponsor Name:ASISTANCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
Full Title: Riluzole for the treatment of spasticity in the traumatic chronic spinal cord injury condition: Adaptive, Multicenter, placebo-controlled, randomised, double blind trial in a Rare Disorder” RILUSCI | ||
Medical condition: the traumatic chronic spinal cord injury condition | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000948-98 | Sponsor Protocol Number: H-3-2011-154 | Start Date*: 2012-05-03 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Effect of epinephrine on systemic absorption of mepivacaine administered for brachial plexus block in patients with end-stage renal disease | |||||||||||||
Medical condition: End-stage renal disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002924-11 | Sponsor Protocol Number: LOLAbiome | Start Date*: 2023-01-09 | ||||||||||||||||
Sponsor Name:CBmed GmbH | ||||||||||||||||||
Full Title: An observational study on the effect of L-ornithine-L-aspertate (LOLA) on the Flavonifractor abundance in the gut microbiome in liver cirrhosis | ||||||||||||||||||
Medical condition: Liver cirrhosis with covert or overt hepatic encephalopathy (grade 0-2) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005271-16 | Sponsor Protocol Number: 2010NE02 | Start Date*: 2012-11-29 | |||||||||||
Sponsor Name:University of Dundee & NHS Tayside | |||||||||||||
Full Title: Does oral sodium bicarbonate therapy improve function and quality of life in older patients with chronic kidney disease and low-grade acidosis? A multicentre randomized placebo controlled trial | |||||||||||||
Medical condition: Chronic kidney disease stages 4/5 with metabolic acidosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002755-42 | Sponsor Protocol Number: MRX-800 | Start Date*: 2020-03-16 | |||||||||||||||||||||
Sponsor Name:Mirum Pharmaceuticals Inc. | |||||||||||||||||||||||
Full Title: MRX-800: A Long-Term Safety Study of Maralixibat, an Apical Sodium Dependent Bile Acid Transporter Inhibitor (ASBTi), in the Treatment of Cholestatic Liver Disease in Subjects Who Previously Partic... | |||||||||||||||||||||||
Medical condition: Long-term safety study with Maralixibat, in treatment of subjects with cholestatic liver disease including, but not limited to, Alagille syndrome (ALGS) and Progressive Familial Intrahepatic Choles... | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) PL (Completed) FR (Completed) ES (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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