- Trials with a EudraCT protocol (228)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (16)
228 result(s) found for: Botulinum Toxin Type A.
Displaying page 6 of 12.
EudraCT Number: 2004-002369-19 | Sponsor Protocol Number: 11.8.2004 | Start Date*: 2004-10-12 |
Sponsor Name:Hvidovre Hospital [...] | ||
Full Title: Behandling af savlen hos børn med cerebral parese ved anvendelse af botulinum toksin i spytkirtler | ||
Medical condition: Børn med cerebral parese har ofte problemer med savlen, primært på grund af nedsat synkefunktion. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005252-40 | Sponsor Protocol Number: BTX0507 | Start Date*: 2005-12-15 |
Sponsor Name:Aalst Dermatology Group | ||
Full Title: A Prospective Evaluation of BOTOX® and Dysport® in Temporal Brow Elevation | ||
Medical condition: For subjects who desire brow lift as a means to rejuvenate the upper face. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023240-33 | Sponsor Protocol Number: POPPIES | Start Date*: 2011-04-21 | ||||||||||||||||
Sponsor Name:Guys and St Thomas' NHS Foundation Trust | ||||||||||||||||||
Full Title: Post-operative pain in children with cerebral palsy following major hip surgery: a double blind randomised placebo controlled trial of pre-operative Botulinum toxin type A. [The Post-Operative Pain... | ||||||||||||||||||
Medical condition: Post Operative Pain in Cerebral Palsy | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003231-30 | Sponsor Protocol Number: Linitox | Start Date*: 2018-10-19 | ||||||||||||||||||||||||||
Sponsor Name:Aránzazu Vázquez Doce | ||||||||||||||||||||||||||||
Full Title: EFFECTIVENESS OF THE REPEATED INFILTRATIONS OF BOTULINUM TOXIN A IN THE GAIT AND QUALITY OF LIFE IN ADULTS WITH SPASTIC PARAPARESIA SECONDARY TO MULTIPLE SCLEROSIS | ||||||||||||||||||||||||||||
Medical condition: Multiple sclerosis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004890-25 | Sponsor Protocol Number: BOLD01 | Start Date*: 2013-01-14 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA S. MARIA DELLA MISERICORDIA DI UDINE | |||||||||||||
Full Title: Botulinum Toxin Serotype A randomized double-blind, placebo controlled multicentre study for degenerative coxarthrosis. | |||||||||||||
Medical condition: coxarthrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000575-32 | Sponsor Protocol Number: 1 | Start Date*: 2018-12-18 | |||||||||||
Sponsor Name:Isabel Maria Ruiz | |||||||||||||
Full Title: Results of the injection of botulinum toxin vs platelet rich plasma for the treatment of plantar fasciitis | |||||||||||||
Medical condition: Plantar fasciitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003939-38 | Sponsor Protocol Number: P160404J | Start Date*: 2017-12-19 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Short-term efficacy of a single ultrasound-guided intra-articular injection of botulinum toxin A associated with splinting for base-of-thumb osteoarthritis on pain at 3 months: A randomized placebo... | |||||||||||||
Medical condition: Patients referred to our Physical Medicine Rehabilitation Department of a tertiary care center in Paris, France, for the management of Base-of-thumb osteoarthritis (BTOA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001063-12 | Sponsor Protocol Number: EVB-003 | Start Date*: 2015-04-22 | |||||||||||
Sponsor Name:Evolus Inc. | |||||||||||||
Full Title: A phase III, multi-center, randomized, double blind, active and placebo control, single dose trial to demonstrate the efficacy and safety of DWP-450 in adult subjects for treatment of moderate-to-s... | |||||||||||||
Medical condition: moderate-to-severe glabellar lines | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003148-21 | Sponsor Protocol Number: BASICstudy | Start Date*: 2019-01-25 |
Sponsor Name:NTNU- Norwegian University of Science and Technology | ||
Full Title: BASIC - Botulinum toxin type A blockade of the sphenopalatine ganglion in treatment-refractory chronic cluster headache | ||
Medical condition: Chronic cluster headache | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001639-35 | Sponsor Protocol Number: M602011014 | Start Date*: 2019-11-26 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: Prospective, randomized, double-blind, placebo-controlled, multicenter study to investigate the efficacy and safety of NT 201 in the treatment of lower limb spasticity caused by stroke or traumatic... | |||||||||||||
Medical condition: Diagnosis of lower limb spasticity with or without upper limb spasticity of the same body side caused by stroke or traumatic brain injury | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) DE (Trial now transitioned) FR (Trial now transitioned) NO (Completed) CZ (Trial now transitioned) GB (GB - no longer in EU/EEA) ES (Ongoing) IT (Trial now transitioned) HU (Trial now transitioned) SK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020886-26 | Sponsor Protocol Number: MRZ60201_3053_1 | Start Date*: 2011-12-15 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: Prospective, open-label, non-randomized, single-arm, multi-center dose titration study to investigate the safety and efficacy of NT 201 in subjects deemed to require total body doses of 800 U of NT... | |||||||||||||
Medical condition: Spasticity of the upper and lower limb of the same body side due to cerebral causes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) PT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000697-23 | Sponsor Protocol Number: MRZ 60201-0703/1 | Start Date*: 2007-07-10 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: Prospective, single-arm, single-center, open-label trial to investigate the tolerability of NT 201 and quality of life of patients in the treatment of blepharospasm with shortened injection intervals | |||||||||||||
Medical condition: Blepharospasm | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004399-68 | Sponsor Protocol Number: 1925-201-008 | Start Date*: 2019-03-29 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A Phase 2, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Dose Ranging Study to Evaluate the Efficacy and Safety of Botulinum Toxin Type A (AGN 151607) Injections into the Epicardial F... | |||||||||||||
Medical condition: Post-operative atrial fibrillation (POAF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) AT (Completed) SE (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004834-42 | Sponsor Protocol Number: 191622-057-02 | Start Date*: 2006-09-11 | |||||||||||
Sponsor Name:Allergan | |||||||||||||
Full Title: A Multi-Center, Double-Blind, Placebo-Controlled, Parallel Group Safety Study of Pulmonary Function in Patients with Reduced Lung Function Treated with BOTOX® (Botulinum Toxin Type A) Purified Neur... | |||||||||||||
Medical condition: Focal upper limb spasticity due to upper motor neuron syndrome including poststroke spasticity. (for the objective of this study patients must also have stable compromised baseline respiratory status) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003471-30 | Sponsor Protocol Number: D-FR-52120-222 | Start Date*: 2016-09-26 | |||||||||||
Sponsor Name:Ipsen Innovation | |||||||||||||
Full Title: A PHASE III, MULTICENTRE, RANDOMISED, DOUBLE BLIND, PARALLEL GROUP, PLACEBO CONTROLLED STUDY TO ASSESS THE EFFICACY AND SAFETY OF ONE OR MORE INTRADETRUSOR TREATMENTS OF 600 OR 800 UNITS OF DYSPORT... | |||||||||||||
Medical condition: Urinary incontinence (UI) caused by neurogenic detrusor overactivity due to either spinal cord injury or multiple sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Completed) PT (Completed) CZ (Completed) IT (Completed) NL (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000919-29 | Sponsor Protocol Number: TB2006 | Start Date*: 2006-12-20 | |||||||||||
Sponsor Name:ISTITUTI ORTOPEDICI RIZZOLI | |||||||||||||
Full Title: Study on reversible effect on muscle of the botulinica toxin on the prevention of the post-traumatic rigidity of elbow | |||||||||||||
Medical condition: omero mono-Inter-sovra-sovraintercondiloidee fractures of distant them, fractures of capitello radial and fractures of olecrano with or without luxation | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001013-81 | Sponsor Protocol Number: ProBaBle | Start Date*: 2014-10-10 | |||||||||||
Sponsor Name:Centro Hospitalar de São João, EPE | |||||||||||||
Full Title: Treatment of Bladder Pain Syndrome with Onabotulinum toxin A | |||||||||||||
Medical condition: Bladder Pain Syndrome | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006048-29 | Sponsor Protocol Number: INjECT | Start Date*: 2022-02-21 | ||||||||||||||||
Sponsor Name:AOU MATERDOMINI | ||||||||||||||||||
Full Title: BotulInum toxin type A for peripheral Neuropathic pain in subjEcts with Carpal Tunnel syndrome: a multicenter, randomized, double-blind, placebo-controlled study | ||||||||||||||||||
Medical condition: Peripheral neuropathic pain in subjects with carpal tunnel syndrome | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000073-29 | Sponsor Protocol Number: MRZ 60201-0528/1 | Start Date*: 2006-07-10 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: Prospective, randomised, double-blind, placebo-controlled multicentre pilot trial to investigate the impact of an early use of NT 201 in patients with an acute cerebrovascular event on the developm... | |||||||||||||
Medical condition: Patients with acute cerebrovascular event showing signs of beginning upper limb spasticity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005114-33 | Sponsor Protocol Number: s57283 | Start Date*: 2015-03-10 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: Effectiveness of Botulinum Toxin Infiltration for treatment of upper limb dysfunctions after treatment for breast cancer | |||||||||||||
Medical condition: The aim of this study is to examine the effect of Botolinum Toxine infiltration in the pectoral muscle, in combination with an individual physical therapy programme, on pain and upper limb dysfunct... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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