- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11 result(s) found for: Facial paralysis.
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EudraCT Number: 2009-018143-25 | Sponsor Protocol Number: 2010 | Start Date*: 2010-05-06 | ||||||||||||||||
Sponsor Name:Västra Götalandsregionen | ||||||||||||||||||
Full Title: An open label, historical control, study to assess the impact on bacteriological healing of Prednisolone in patients with neuroborreliosis-caused peripheral facial palsy receiving treatment with Do... | ||||||||||||||||||
Medical condition: Facialispares orsakad av CNS-infektion med Borrelia burgdorferi. (Neuroborrelios-orsakad facialispares) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005658-66 | Sponsor Protocol Number: P051072 | Start Date*: 2006-12-27 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Evaluation de l'efficacité des corticoïdes dans la prévention de la paralysie faciale après chirurgie d'exérése d'une tumeur du méat auditif interne et /ou de l'angle ponto-cérébelleux | |||||||||||||
Medical condition: Prévention de la paralysie faciale après chirurgie d'éxérèse d'une tumeur du méat auditif interne et/ou de l'angle ponto-cérébelleux. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004696-12 | Sponsor Protocol Number: FACIALPARALYSIS | Start Date*: 2020-01-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA INTEGRATA VERONA | |||||||||||||
Full Title: Clinical, Instrumental and Histological evaluation of the combined use of Onabotulinumtoxin A and hyaluronic acid fillers in patients with facial paralysis | |||||||||||||
Medical condition: hemifacial paralysis (3 to 6 of the House-Brackmann scale) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004187-35 | Sponsor Protocol Number: FACE-01 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Falun Hospital | |||||||||||||
Full Title: The FACE (Facial nerve palsy And Cortisone Evaluation) study in children: a randomised double-blind, placebo-controlled, multicenter trial. | |||||||||||||
Medical condition: Facial Nerve Palsy (Bells Palsy) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005215-46 | Sponsor Protocol Number: VS_Nimodipine | Start Date*: 2021-02-19 |
Sponsor Name:Department of Neurosurgery, Medical University of Vienna | ||
Full Title: Intraoperative application of nimodipine to the facial and cochlear nerves during vestibular schwannoma resection to avoid spasm-related postoperative facial paralysis and deafness - a prospective ... | ||
Medical condition: Patients with vestibularis schwanomma undergoing microsurgical resection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004636-66 | Sponsor Protocol Number: KP-2011-0077 | Start Date*: 2011-12-05 |
Sponsor Name:Uppsala University Hospital | ||
Full Title: Single-blinded randomized trial of Botulinumtoxin A (Vistabel®) and its objective paralytic effect in the facial muscles of healthy women: development of new neurophysiological measurements. | ||
Medical condition: The treatment of glabellar lines in healthy women by muscle paralysis from injection of botulinum toxin | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002952-17 | Sponsor Protocol Number: CVL-751-PD-004 | Start Date*: 2021-03-30 | |||||||||||
Sponsor Name:Cerevel Therapeutics, LLC | |||||||||||||
Full Title: 58-Week Open-label Trial of Tavapadon in Parkinson’s Disease (TEMPO-4 Trial) | |||||||||||||
Medical condition: Patients (40 to 80 years age) who have diagnosis of Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) CZ (Trial now transitioned) HU (Trial now transitioned) IT (Trial now transitioned) BG (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003017-14 | Sponsor Protocol Number: 132998 | Start Date*: 2008-01-08 |
Sponsor Name:Käkkliniken, Universitetssjukhuset i Linköping | ||
Full Title: A comparison of the effect of Atropine and Botulinum-toxin in patients with severe drooling | ||
Medical condition: Patients with ALS, Parkinson´s disease, brain-damage cerebral paralysis or other neurological conditions often have an impaired swallowing, resulting in drooling. This adds a social handicap and o... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000749-21 | Sponsor Protocol Number: 4.20 | Start Date*: 2016-03-14 |
Sponsor Name:Medizinische Hochschule Hannover | ||
Full Title: Botulinumtoxin A for emotional stabilization in borderline personality disorder | ||
Medical condition: Borderline personality disorder | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-001300-30 | Sponsor Protocol Number: 2017_CERVPLEX_1.1 | Start Date*: 2017-10-03 |
Sponsor Name:UK für Anästhesieologie, Gemeinn. Sbg. Landeskliniken BetriebsgesmbH | ||
Full Title: Comparison of deep, intermediate and superficial cervical plexus block for carotid endarterectomies concerning paresis of the phrenic nerve, lung function and tissue distribution: a prospective, ra... | ||
Medical condition: deep, intermediate or superficial cervical plexus block for carotid endarterectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-006067-28 | Sponsor Protocol Number: CST103/CST107-CLIN-011 | Start Date*: 2022-01-10 | ||||||||||||||||||||||||||
Sponsor Name:CuraSen Therapeutics, Inc. | ||||||||||||||||||||||||||||
Full Title: A Phase II, Randomized, Placebo-Controlled, Double-Blind, Crossover, Study of the Pharmacodynamic Effects of CST-103 co-administered with CST-107 on the Central Nervous System in Subjects with Neur... | ||||||||||||||||||||||||||||
Medical condition: Patients with Parkinson’s Disease with REM sleep behaviour disorder, Mild Cognitive Impairment, Dementia with Lewy Bodies and Parkinson’s Disease Dementia. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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