- 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 4 of 12.
EudraCT Number: 2017-003117-25 | Sponsor Protocol Number: V3.0 | Start Date*: 2018-05-17 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Longitudinal chemodenervation effects of botulinum toxin A after intramuscular application and the impact of physical activity | ||
Medical condition: Spastic hemiparesis with involvement of the M. biceps brachii | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002086-20 | Sponsor Protocol Number: A-94-52120-098 | Start Date*: 2005-03-09 |
Sponsor Name:Ipsen Pharma GmbH | ||
Full Title: Open, multicentre study on the equivalent efficacy and safety of Botulinum toxin A (500 Units Dysport®) in the treatment of heterogeneous forms of cervical dystonia | ||
Medical condition: Cervical dystonia (CD), one of the most common forms of focal dystonia, is characterised by an altered head posture, pain in the the neck and shoulder region and hypertrophy of the concerned muscle... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-018345-64 | Sponsor Protocol Number: 38/10 | Start Date*: 2011-03-23 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Evaluation of the efficacy of Xeomin in the treatment of cervical dystonia (CD) and blepharospasmus (BS) in patients who did not respond to treatment with Botox. | ||||||||||||||||||
Medical condition: cervical dystonia, blepharospasmus (BS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004704-35 | Sponsor Protocol Number: BTX1-myalgia_pain | Start Date*: 2020-05-18 |
Sponsor Name:Region Örebro | ||
Full Title: Masseter myofascial pain relief following an intra-muscular injection with botulinum toxin type A. A randomized double-blind controlled multicenter pilot study. | ||
Medical condition: Myalgia of jaw muscle | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-004377-33 | Sponsor Protocol Number: 011015-01 | Start Date*: 2016-04-13 |
Sponsor Name:Department of Neuroscience, NTNU | ||
Full Title: Botulinum toxin type A Block for the sphenopalatine ganglion in chronic rhinosinusitis With nasal polyposis | ||
Medical condition: Chronic rhinosinusitis with nasal polyposis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000833-36 | Sponsor Protocol Number: STH14330 | Start Date*: 2007-12-14 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: The Action of Botox® on Urgency – A precise evaluation of its impact on urodynamic parameters during bladder filling in patients with non-neurogenic Overactive Bladder (OAB). | |||||||||||||
Medical condition: Non-neurogenic Overactive Bladder (OAB) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001709-33 | Sponsor Protocol Number: P160926J | Start Date*: 2017-10-27 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Randomized, Double-blind, Placebo-controlled Trial on the Efficacy of the Botulinum Toxin for the Treatment of Lateral Epicondylitis | |||||||||||||
Medical condition: Patients suffering from unilateral lateral epicondylitis, persistent for more than 3 months or recurrent and not having responded to at least one reference treatment | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019085-82 | Sponsor Protocol Number: Y-52-52120-146 | Start Date*: 2011-02-24 | |||||||||||
Sponsor Name:Ipsen Innovation | |||||||||||||
Full Title: A PHASE II, DOUBLE BLIND, RANDOMISED, PLACEBO AND ACTIVE COMPARATOR CONTROLLED STUDY TO ASSESS THE SAFETY AND EFFICACY OF THREE DOSES OF DYSPORT RU (20 U, 50 U AND 75 U) ADMINISTERED AS A SINGLE TR... | |||||||||||||
Medical condition: Moderate to severe glabellar lines | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000240-22 | Sponsor Protocol Number: M21-310 | Start Date*: 2021-11-24 |
Sponsor Name:AbbVie | ||
Full Title: A Phase 3 Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of BOTOX® (Botulinum Toxin Type A) Purified Neurotoxin Complex for the Treatment of Pla... | ||
Medical condition: Moderate and severe platysma prominence | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) DE (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: 2007-005958-23 | Sponsor Protocol Number: Y-47-52120-128 | Start Date*: 2008-03-03 | |||||||||||
Sponsor Name:Ipsen Group, SCRAS Institut Henri Beaufour | |||||||||||||
Full Title: A Phase II, Randomised, Double-Blind Study to Compare the Safety and Efficacy of One Treatment Cycle of Clostridium Botulinum Type A Toxin (50 Units) When Reconstituted from Either a 125 Unit or a ... | |||||||||||||
Medical condition: Moderate to severe vertical glabellar lines. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023043-15 | Sponsor Protocol Number: MRZ60201/SP/3001 | Start Date*: 2011-09-14 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: Prospective, double-blind, placebo-controlled, randomized, multi-center study with an open-label extension period to investigate the efficacy and safety of NT 201 in the treatment of post-stroke sp... | |||||||||||||
Medical condition: post-stroke spasticity of the upper limb | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005568-24 | Sponsor Protocol Number: 214-06/06 | Start Date*: 2007-03-29 | |||||||||||
Sponsor Name:Dermatologikum Hamburg | |||||||||||||
Full Title: Prüfung der Wirksamkeit und der Verträglichkeit von Botulinum-Toxin (Xeomin®) in verschiedenen Verdünnungen Evaluation of the Efficacy and Safety of Botulinumtoxin (Xeomin®) in different dilutions | |||||||||||||
Medical condition: Moderate to severe glabellar frown lines | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000326-19 | Sponsor Protocol Number: BX-Stolav-0216 | Start Date*: 2016-12-02 |
Sponsor Name:St Olavs Hospital Trondheim University Hospital | ||
Full Title: Treatment of obesity in adolescents by endoscopic injection of Botulinum toxin A - A randomised, double blind, placebo-controlled phase II-trial followed by an open-label cohort-controlled extension | ||
Medical condition: Obesity | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024579-23 | Sponsor Protocol Number: MRZ60201/SP/3002 | Start Date*: 2012-02-06 | |||||||||||
Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
Full Title: Prospective, double-blind, placebo-controlled, randomized, multi-center study with an open-label extension period to investigate the efficacy and safety of NT 201 in the treatment of post-stroke sp... | |||||||||||||
Medical condition: post-stroke spasticity of the lower limb | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) CZ (Completed) ES (Completed) PL (Completed) IT (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001378-29 | Sponsor Protocol Number: RAE02 | Start Date*: 2005-05-23 |
Sponsor Name:Bradford Teaching Hospitals NHS Foundation Trust | ||
Full Title: A double blinded randomised controlled trial of injection of botulinum toxin versus normal saline into the puborectalis muscle in patients with pelvic floor dyssynergia. | ||
Medical condition: Obstructed defeacation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002210-23 | Sponsor Protocol Number: 1.4botox | Start Date*: 2014-10-14 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Can local intramuscular botulinum toxin improve dysphagia in patients with myopathic dysphagia and constriction of the cricoid muscle? | |||||||||||||
Medical condition: Oculopharyngesl muscle dystrophy, inclusion body myositis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000877-10 | Sponsor Protocol Number: MWTBTXA | Start Date*: 2021-07-14 | |||||||||||
Sponsor Name:Bispebjerg Hospital, Department of Dermatology | |||||||||||||
Full Title: Longevity of microwave thermolysis and botulinum toxin A for treatment of axillary hyperhidrosis: a randomized intra-individual trial | |||||||||||||
Medical condition: Axillary hyperhidrosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006001-35 | Sponsor Protocol Number: PREBOT-II | Start Date*: 2021-10-27 | |||||||||||
Sponsor Name:University Hospital Heidelberg | |||||||||||||
Full Title: Randomized controlled trial of PREoperative injection of BOTulinum toxin into the sphincter of Oddi to reduce bile leakage after hepatic resection PREBOT-II | |||||||||||||
Medical condition: Patients undergoing partial hepatic resection for various underlying diseases. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000642-22 | Sponsor Protocol Number: SEMG | Start Date*: 2017-07-19 |
Sponsor Name:Jose Alberola-Rubio | ||
Full Title: Electromyographic study for the help and guidance of Botox administration in the treatment of chronic pelvic floor pain | ||
Medical condition: Chronic pelvic pain | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
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