- Trials with a EudraCT protocol (126)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (35)
126 result(s) found for: Spasticity.
Displaying page 2 of 7.
EudraCT Number: 2019-003559-12 | Sponsor Protocol Number: INCIPIT | Start Date*: 2021-01-27 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA INTEGRATA VERONA | ||||||||||||||||||
Full Title: Prospective, open-label, non-randomized, single-arm, dose titration study to investigate the efficacy and safety of IncobotulinumtoxinA in children deemed to require a total body dose up to 22U/kg ... | ||||||||||||||||||
Medical condition: Multifocal spasticity of the upper and lower limb due to cerebral palsy | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-004127-40 | Sponsor Protocol Number: ESPSEVMOLIN2022 | Start Date*: 2023-05-03 |
Sponsor Name:Dra. Nuria Gutierrez Dubón | ||
Full Title: Clinical trial on the effectiveness and safety of botulinum toxin type A (incobotulinumtoxin) in doses adapted to the individual needs of patients with severe spasticity | ||
Medical condition: brain damage oriented spasticity | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005910-11 | Sponsor Protocol Number: GWSP0604 | Start Date*: 2007-08-29 |
Sponsor Name:GW Pharma Ltd | ||
Full Title: A two-phase Phase 3 study of the safety and efficacy of Sativex®, in the symptomatic relief of spasticity in subjects with spasticity due to multiple sclerosis: Phase A – single blind response asse... | ||
Medical condition: Spacticity in multiple sclerosis (MS) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) GB (Completed) ES (Completed) DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004497-33 | Sponsor Protocol Number: Protocol_Dysport_v3__13.12.2017 | Start Date*: 2018-03-06 | |||||||||||||||||||||
Sponsor Name:Copenhagen University Hospital at Hvidovre | |||||||||||||||||||||||
Full Title: Measuring effects on pain and quality of life after Dysport® injection in children with cerebral palsy | |||||||||||||||||||||||
Medical condition: Muscle pain in the extremities due to spasticity in children with cerebral palsy | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002509-63 | Sponsor Protocol Number: GWCL0403 | Start Date*: 2005-03-11 |
Sponsor Name:GW Pharma Ltd | ||
Full Title: A double blind, randomised, placebo controlled, parallel group study of Sativex, in subjects with symptoms of spasticity due to multiple sclerosis | ||
Medical condition: Spasticity due to Multiple Sclerosis (MS) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011216-38 | Sponsor Protocol Number: 1.02.7001 | Start Date*: 2009-09-01 | |||||||||||
Sponsor Name:Medtronic International Trading Sarl | |||||||||||||
Full Title: A randomized, controlled, open-label, parallel-group, multicenter study to compare the effect of Intrathecal Baclofen Therapy (ITB Therapy) versus Best Medical Treatment (BMT) on severe spasticity ... | |||||||||||||
Medical condition: Severe spasticity in post-stroke patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) ES (Completed) BE (Completed) DE (Completed) IT (Completed) NL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002346-37 | Sponsor Protocol Number: 191622-127 | Start Date*: 2014-05-21 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: BOTOX® Treatment in Adult Patients with Upper Limb Spasticity | |||||||||||||||||||||||
Medical condition: Poststroke spasticity involving the muscles of the elbow and shoulder in adult patients | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002327-42 | Sponsor Protocol Number: 191622-129 | Start Date*: 2014-05-21 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: Long-term Study of BOTOX® Treatment in Adult Patients with Upper Limb Spasticity | |||||||||||||||||||||||
Medical condition: Poststroke spasticity involving the muscles of the elbow and shoulder in adult patients | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005197-78 | Sponsor Protocol Number: 1 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Queen's Medical Centre, Nottingham, University Hospital NHS Trust, | |||||||||||||
Full Title: A multi-centre, randomised, parallel group, cross-over study comparing the efficacy and safety of double versus multiple injections of Botulinum Toxin type-A (Dysport®), into the gastrocnemius musc... | |||||||||||||
Medical condition: Spasticity of the Gastrocnemius Muscle due to Cerebral Palsy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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: 2021-001634-18 | Sponsor Protocol Number: M602011072 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||||||||||||
Full Title: A prospective, randomized, double-blind, placebo-controlled, two-stage, multicenter study with an open-label extension period to investigate the efficacy and safety of NT 201 in the treatment of lo... | |||||||||||||||||||||||
Medical condition: Pediatric lower limb (LL) spasticity (SP) caused by cerebral palsy (CP) | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Trial now transitioned) LV (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005055-17 | Sponsor Protocol Number: MRZ60201_3071_1 | Start Date*: 2013-09-26 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: Open-label, non-controlled, multicenter long-term study to investigate the safety and efficacy of Xeomin® (incobotulinumtoxin A, NT 201) for the treatment of spasticity of the lower limb(s) or of c... | |||||||||||||
Medical condition: Lower limb and combined lower limb and upper limb spasticity due to cerebral palsy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) EE (Completed) SK (Completed) CZ (Completed) Outside EU/EEA FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000236-16 | Sponsor Protocol Number: IPX056-B06-03 | Start Date*: 2007-05-28 | |||||||||||
Sponsor Name:IMPAX Laboratories, Inc. | |||||||||||||
Full Title: A Double-Blind, Randomized, Placebo- and Active Comparator- Controlled, Parallel Group, Multinational Study to Evaluate the Pharmacokinetics and Pharmacodynamics of IPX056 in Subjects with Establis... | |||||||||||||
Medical condition: Established Spasticity Resulting from Multiple Sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004100-22 | Sponsor Protocol Number: OS440-3004 | Start Date*: 2018-03-16 | |||||||||||
Sponsor Name:Osmotica Pharmaceutical US LLC | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Parallel Group Study to Investigate the Safety and Efficacy of Arbaclofen Extended-Release Tablets for the Treatment of Spasticity in Patients with Mu... | |||||||||||||
Medical condition: Spasticity in patients with multiple sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) PL (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022808-40 | Sponsor Protocol Number: CANALS | Start Date*: 2011-01-13 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
Full Title: A fase II, randomized, Double-Blind, Placebo-Controlled, Multicentre Study for the Safety and Efficacy on Spasticity Symptoms of a Cannabis Sativa Extract in Motor Neuron Disease Patients | |||||||||||||
Medical condition: amyotrophic lateral sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001356-22 | Sponsor Protocol Number: CLR_09_21 | Start Date*: 2016-07-13 | |||||||||||
Sponsor Name:Sun Pharma Advanced Research Company Ltd. | |||||||||||||
Full Title: A PLACEBO-CONTROLLED RANDOMIZED WITHDRAWAL EVALUATION OF THE EFFICACY AND SAFETY OF BACLOFEN ER CAPSULES (GRS) IN SUBJECTS WITH SPASTICITY DUE TO MULTIPLE SCLEROSIS | |||||||||||||
Medical condition: Spasticity due to multiple sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015868-34 | Sponsor Protocol Number: Y-55-52120-140 | Start Date*: 2011-02-15 | |||||||||||
Sponsor Name:Ipsen Pharma SAS | |||||||||||||
Full Title: A PHASE III, MULTICENTRE, DOUBLE BLIND, PROSPECTIVE, RANDOMISED, PLACEBO CONTROLLED STUDY, ASSESSING THE EFFICACY AND SAFETY OF DYSPORT USED FOR THE TREATMENT OF LOWER LIMB SPASTICITY IN ADULT SUBJ... | |||||||||||||
Medical condition: Leg Spasticity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) SK (Completed) IT (Completed) PT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004451-40 | Sponsor Protocol Number: H15/02 | Start Date*: 2016-02-17 | |||||||||||
Sponsor Name:Almirall Hermal GmbH | |||||||||||||
Full Title: SATIVEX® AS ADD-ON THERAPY VS. FURTHER OPTIMIZED FIRST-LINE ANTISPASTICS THE S A V A N T TRIAL | |||||||||||||
Medical condition: Moderate to severe spasticity due to MS (multiple sclerosis). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017723-26 | Sponsor Protocol Number: Y5552120142 | Start Date*: 2011-04-28 | |||||||||||
Sponsor Name:Ipsen Pharma SAS | |||||||||||||
Full Title: A phase III, prospective, multicentre, open label, extension study, to assess the long term safety and efficacy of repeated treatment of Dysport® intramuscular injection in the treatment of lower l... | |||||||||||||
Medical condition: Leg Spasticity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) SK (Completed) IT (Completed) PT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004101-40 | Sponsor Protocol Number: OS440-3005 | Start Date*: 2018-03-23 | |||||||||||
Sponsor Name:Osmotica Pharmaceutical US LLC | |||||||||||||
Full Title: An Open-Label Study to Evaluate the Long-Term Safety of Arbaclofen Extended-Release Tablets in Multiple Sclerosis Patients with Spasticity (Study OS440-3005). | |||||||||||||
Medical condition: Spasticity in patients with multiple sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) PL (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
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