- 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... | ||||||||||||||||||
|
||||||||||||||||||
| 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 | |||||||||||||
|
|||||||||||||
| 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) | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
| 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... | |||||||||||||
|
|||||||||||||
| 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: View results | ||
| 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 | |||||||||||||
|
|||||||||||||
| 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... | |||||||||||||
|
|||||||||||||
| 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) | |||||||||||||
|
|||||||||||||
| 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). | |||||||||||||
|
|||||||||||||
| 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 | |||||||||||||
|
|||||||||||||
| 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 | |||||||||||||
|
|||||||||||||
| 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 | |||||||||||||
|
|||||||||||||
| 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 | |||||||||||||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.