- Trials with a EudraCT protocol (64)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
64 result(s) found for: Neuromuscular system.
Displaying page 1 of 4.
EudraCT Number: 2013-002362-39 | Sponsor Protocol Number: TALVISUG01 | Start Date*: 2013-11-21 | ||||||||||||||||
Sponsor Name:Consorci Mar Parc de Parc de Salut de Barcelona (Parc de Salut MAR) | ||||||||||||||||||
Full Title: Reducing the dose of sugammadex 50% reverse the neuromuscular blockade of rocuronium effectively after general anesthesia. | ||||||||||||||||||
Medical condition: Neuromuscular blockade is induced during general anesthesia, which often does not recover spontaneously, so it is necessary a pharmacological reversal. We believe that sugammadex at lower doses tha... | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006704-27 | Sponsor Protocol Number: Bezafibrate | Start Date*: 2009-07-17 | |||||||||||
Sponsor Name:Neuromuscular Research Unit, Copenhagen University Hospital Rigshopspitalet | |||||||||||||
Full Title: Effect of Bezafibrate on muscle metabolism during exercise in patients with fat metabolic disorders in skeletal muscle | |||||||||||||
Medical condition: Evaluation of the effect of Bezafibrate on muscle metabolism during exercise in patients with VLCAD and CPT II deficiency | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022558-18 | Sponsor Protocol Number: 2010-022558-18 | Start Date*: 2010-10-11 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA | ||||||||||||||||||||||||||||
Full Title: A pilot trial with clenbuterol in spinal and bulbar muscular atrophy (SBMA). | ||||||||||||||||||||||||||||
Medical condition: spinal and bulbar muscular atrophy (SBMA) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011184-36 | Sponsor Protocol Number: 08/0169 | Start Date*: 2009-07-14 | |||||||||||
Sponsor Name:University College London-Joint UCLH/UCL Biomedical (R&D) Unit | |||||||||||||
Full Title: A Phase II Randomised, Double-Blind, Placebo Controlled, Cross-Over Study to Investigate the Efficacy of Mexiletine in Patients with Non-Dystrophic Myotonia. | |||||||||||||
Medical condition: Non-Dystrophic Myotonia (NDM). Non-dystrophic myotonias are a group of rare neuromuscular disorders that cause episodes of muscle stiffness (known as myotonia) and paralysis. Predominantly the musc... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001622-91 | Sponsor Protocol Number: RKMMS 04 | Start Date*: 2005-06-23 |
Sponsor Name:Royal Group Hospitals | ||
Full Title: A randomised assessor blinded study to examine the role of skin testing in the prediction of peri-operative anaphylaxis and its correlation with mast cell tryptase and total IgE. | ||
Medical condition: Prevalance of sensitivity of immune system to the four named neuromuscular blocking drugs in patients undergoing anaesthesia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000876-27 | Sponsor Protocol Number: ATX-MTM-002 | Start Date*: 2017-12-06 |
Sponsor Name:Audentes Therapeutics Inc. | ||
Full Title: ASPIRO: A Phase 1/2, Randomized, Open-Label, Ascending-Dose, Delayed-Treatment Concurrent Control Clinical Study to Evaluate the Safety and Efficacy of AT132, an AAV8-Delivered Gene Therapy in X-L... | ||
Medical condition: X-linked Myotubular Myopathy (XLMTM) | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | |
Trial protocol: GB (GB - no longer in EU/EEA) DE (Trial now transitioned) FR (Trial now transitioned) | ||
Trial results: View results |
EudraCT Number: 2019-003033-42 | Sponsor Protocol Number: EURO-RELAX | Start Date*: 2020-01-28 |
Sponsor Name:INSTITUTO DE INVESTIGACIÓN SANITARIA LA FE | ||
Full Title: The impact of deep versus standard muscle relaxation on intra-operative safety during laparoscopic surgery: a multicenter strategy study – EURO RELAX STUDY | ||
Medical condition: Intra-operative adverse events during laparoscopic surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002295-40 | Sponsor Protocol Number: 08-06-2018-paracet | Start Date*: 2018-09-11 |
Sponsor Name:Copenhagen Neuromuscular Center | ||
Full Title: Pharmacokinetics and safety of treatment with paracetamol in children and adults with spinal muscular atrophy and cerebral palsy | ||
Medical condition: Spinal muscular atrophy type II (SMA II) Cerebral palsy (CP) | ||
Disease: | ||
Population Age: Children, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003670-40 | Sponsor Protocol Number: PAN.1 | Start Date*: 2018-04-05 |
Sponsor Name:Beatrix Children's Hospital, University Medical Center Groningen | ||
Full Title: Pediatric Ards Neuromuscular blockade (PAN) study: Life-threatening acute respiratory failure in children: to breathe or not to breathe spontaneously, that's the question. | ||
Medical condition: Pediatric Acute Respiratory Distress Syndrome necessitating mechanical ventilation | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000755-97 | Sponsor Protocol Number: EPFL-CNBI-2017-01 | Start Date*: 2017-03-16 |
Sponsor Name:Defitech Chair in Brain-Machine Interface, EPFL | ||
Full Title: Brain-computer interface and neuromuscular stimulation for rehabilitation following chronic stroke | ||
Medical condition: I61 - Intracerebral haemorrhage I63 - Cerebral infarction Chronic condition (at least 10 months after occurrence of cerebrovascular accident) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2012-001777-86 | Sponsor Protocol Number: 91710346.1.2 | Start Date*: 2012-10-23 |
Sponsor Name: | ||
Full Title: Pilot study for classification of attempted movement from the electroencephalogram in healthy participants with a temporary paralysis of one arm induced by local administration of rocuronium | ||
Medical condition: Intraoperative awareness during general anesthesia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001503-33 | Sponsor Protocol Number: 2019PI200 | Start Date*: 2021-07-21 | |||||||||||
Sponsor Name:CHRU de Nancy | |||||||||||||
Full Title: The impact of deep versus standard muscle relaxation on intra-operative safety during laparoscopic surgery: a multicenter strategy study – EURO RELAX STUDY | |||||||||||||
Medical condition: Intra-operative adverse events during laparoscopic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001385-16 | Sponsor Protocol Number: BACTstudy | Start Date*: 2019-11-22 |
Sponsor Name:Clinic for Medicine and rehabilitation, Nord-Trondelag Trust (HNT) | ||
Full Title: Botulinum toxin A in frequent and chronic tension-type headache. A double blind, randomized, placebo-controlled cross-over trial | ||
Medical condition: Frequent and chronic tension-type headache | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000323-27 | Sponsor Protocol Number: CV-0003 | Start Date*: 2017-08-03 | |||||||||||
Sponsor Name:CuraVac Europe SA | |||||||||||||
Full Title: A Multi-center, Randomised, Double-blind, Placebo-controlled, Parallel Group Study to Evaluate the Efficacy of Subcutaneous Injections of the Myasthenia Gravis Active Targeted Immunotherapy CV-MG0... | |||||||||||||
Medical condition: Myasthenia Gravis (MG) is a chronic neuromuscular disorder characterized by weakness and fatigability of skeletal muscles. The underlying defect is a decrease in the number of available acetylcho... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003272-23 | Sponsor Protocol Number: NUBE | Start Date*: 2014-10-24 | |||||||||||
Sponsor Name:Dr. Jordi Montero Homs- Unidad de Neuromuscular- Servicio de Neurología- Hospital Universitario de Bellvitge | |||||||||||||
Full Title: Prospective Pilot Study of the treatment of compression of median nerve neuropathy with Nucleo CMP Forte®. | |||||||||||||
Medical condition: Carpal Tunnel Syndrome (CTS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000177-23 | Sponsor Protocol Number: P170930J | Start Date*: 2021-04-13 |
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
Full Title: IMMUNOTHERAPY WITH INTRAVENOUS IMMUNOGLOBULINS, CYCLOPHOSPHAMIDE AND METHYLPREDNISOLONE IN PATIENTS WITH PARANOPLASTIC SENSITIVE NEURONOPATHIES WITH ANTI-HU ANTIBODIES | ||
Medical condition: Paraneoplastic Neurological Syndromes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000243-27 | Sponsor Protocol Number: BUPROPION2019 | Start Date*: 2019-03-18 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: The effect of bupropion in peripheral neuropathic pain. A randomized, double-blind, placebo-controlled study. | |||||||||||||
Medical condition: Peripheral neuropathic , i.e. painful polyneuropathy, postherpetic neuralgia and pain after nerve injury (traumatic or surgical). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002627-10 | Sponsor Protocol Number: RILUMEX | Start Date*: 2015-11-03 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS ISTITUTO NEUROLOGICO CARLO BESTA | |||||||||||||
Full Title: A randomized, double-blind, controlled, monocenter, pivotal phase IIb study to evaluate the efficacy and safety of riluzole versus mexiletine in patients with non dystrophic myotonia mutated in SCN... | |||||||||||||
Medical condition: NDM patients with mutations in SCN4A or CLCN1 gene | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005749-30 | Sponsor Protocol Number: 2015-00887 | Start Date*: 2016-06-23 | |||||||||||
Sponsor Name:Karolinska Institutet | |||||||||||||
Full Title: A randomized, doubleblind, placebo-controlled multicenter trial to evaluate the safety and efficacy of rituximab (Mabthera) in subjects with new onset myasthenia gravis; the RINOMAX study | |||||||||||||
Medical condition: New onset myasthenia gravis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005496-87 | Sponsor Protocol Number: 161403 | Start Date*: 2015-10-15 | |||||||||||
Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
Full Title: A Phase III Study to Evaluate the Efficacy, Safety, and Tolerability of Immune Globulin Infusion 10% (Human) with Recombinant Human Hyaluronidase (HYQVIA/HyQvia) and Immune Globulin Infusion (Human... | |||||||||||||
Medical condition: Chronic inflammatory demyelinating polyradiculoneuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DK (Completed) DE (Completed) SE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) NO (Completed) SK (Completed) GR (Completed) AT (Completed) PL (Completed) HR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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