- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
4 result(s) found for: quadriplegia.
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EudraCT Number: 2021-004994-30 | Sponsor Protocol Number: NL68837.091.21 | Start Date*: 2022-02-08 |
Sponsor Name:Roessingh | ||
Full Title: Pulmonary function and sleep related disorders during cervical admission of intrathecal baclofen in spinal cord injury; a safety study | ||
Medical condition: Spasticity in patients with spinal cord injury | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002499-42 | Sponsor Protocol Number: Version1on02-02-2018 | Start Date*: 2018-08-29 |
Sponsor Name:Cliniques Universitaires Saint-Luc | ||
Full Title: Evaluation of the effect of repeated injections of high doses of botulinum toxin into the lower limb of spastic brain lesions on functional and biomechanical parameters of walking | ||
Medical condition: Patients with spastic brain lesions. Children with cerebral palsy (CP) and in the hemiplegic adult. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001948-19 | Sponsor Protocol Number: IM101-603 | Start Date*: 2017-02-02 | |||||||||||||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Subcutaneous Abatacept in Adults with Active Primary Sjögrens Syndrome | |||||||||||||||||||||||||||||||||
Medical condition: Adults with moderately to severely Active Primary Sjögrens Syndrome | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) CZ (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000101-37 | Sponsor Protocol Number: IM128-035 | Start Date*: 2017-04-07 | |||||||||||||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||||||||||||
Full Title: A Phase II, Randomized, Multi-Center, Double-Blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of BMS-931699 (lulizumab) or BMS-986142 in Subjects with Moderate to Severe Primary ... | |||||||||||||||||||||||||||||||||
Medical condition: subjects with moderate to severe Sjögren's syndrome | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GR (Completed) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
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