- Trials with a EudraCT protocol (84)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
84 result(s) found for: Muscle Spasticity.
Displaying page 2 of 5.
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: 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: 2022-001777-31 | Sponsor Protocol Number: IG2021370 | Start Date*: 2023-05-08 |
Sponsor Name:Hospital de Neurorrehabilitación Institut Guttmann | ||
Full Title: Pilot study on the effect of cannabinoids THC + CBD on resistant spasticity in patients with chronic spinal cord injury. | ||
Medical condition: Pilot study on the effect of THC+CBD cannabinoids on resistant spasticity in patients with chronic spinal cord injury. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
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: 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: 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: 2020-003271-18 | Sponsor Protocol Number: GWSP20105 | Start Date*: 2021-06-07 | ||||||||||||||||
Sponsor Name:GW Pharma Limited | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, 2-way Crossover Trial to Evaluate the Effect of Nabiximols Oromucosal Spray on Clinical Measures of Spasticity in Patients with Multiple Sclerosis | ||||||||||||||||||
Medical condition: Symptomatic treatment of spasticity in patients with multiple sclerosis (MS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
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: 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: 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: 2019-002625-29 | Sponsor Protocol Number: GWSP19066 | Start Date*: 2020-01-14 | ||||||||||||||||
Sponsor Name:GW Pharma Limited | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, 2-way Crossover Trial to Evaluate the Effect of Nabiximols Oromucosal Spray on Clinical Measures of Spasticity in Patients with Multiple Sclerosis | ||||||||||||||||||
Medical condition: Symptomatic treatment of spasticity in patients with multiple sclerosis (MS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
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: 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: 2010-021257-39 | Sponsor Protocol Number: PB-PG-0808-16319 | Start Date*: 2011-07-26 |
Sponsor Name:SWBH NHS Trust [...] | ||
Full Title: Is it clinically effective to treat arm flexor spasticity, with Botulinum toxin – type A (BoNTA) and physiotherapy, as soon as signs of abnormal muscle activity are observed? (A phase II study) | ||
Medical condition: Stroke.Spasticity. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-003623-42 | Sponsor Protocol Number: D-FR-10200-001 | Start Date*: 2021-02-17 | |||||||||||
Sponsor Name:Ipsen Innovation | |||||||||||||
Full Title: An Integrated Phase I/II, Multicentre, Double-Blind, Randomised, Dysport and Placebo-Controlled, Dose-Escalation and Dose-Finding Study to Evaluate the Safety and Efficacy of IPN10200 in the Treatm... | |||||||||||||
Medical condition: Upper limb spasticity after stroke or traumatic brain injury. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) DE (Trial now transitioned) AT (Trial now transitioned) HU (Trial now transitioned) BG (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019162-83 | Sponsor Protocol Number: Y5252120148 | Start Date*: 2011-06-07 | |||||||||||
Sponsor Name:Ipsen Innovation | |||||||||||||
Full Title: A phase III, multicentre, prospective, open label extension study to assess the long term safety and efficacy of repeated treatment of Dysport intramuscular injections used for the treatment of upp... | |||||||||||||
Medical condition: Arm spasticity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) SK (Completed) PL (Completed) IT (Completed) HU (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: 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: 2022-000788-30 | Sponsor Protocol Number: 1.2022 | Start Date*: 2023-04-13 |
Sponsor Name:Uzdrowisko Kamień Pomorski S.A. | ||
Full Title: Evaluation of the effectiveness of Methocarbamol in the treatment of spasticity in people with spinal cord injury. | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Prematurely Ended) | ||
Trial results: (No results available) |
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 |
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