- Trials with a EudraCT protocol (158)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
158 result(s) found for: Sensory system.
Displaying page 1 of 8.
EudraCT Number: 2019-002827-14 | Sponsor Protocol Number: TreatSPG11 | Start Date*: 2021-01-19 | |||||||||||
Sponsor Name:IRCCS Fondazione Stella Maris | |||||||||||||
Full Title: Phase 2 pharmacological experimental study to test the safety of miglustat in subjects with hereditary spastic paraplegia type 11 | |||||||||||||
Medical condition: Spastic paraparesis type 11 (SPG11), caused by mutations in spatacsin protein, is characterized by the association of peripheral neuropathy, parkinsonism, ataxia, cognitive impairment, hypotrophy o... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000902-82 | Sponsor Protocol Number: D8000-003 | Start Date*: 2022-05-24 | |||||||||||
Sponsor Name:Alzecure Pharma AB | |||||||||||||
Full Title: A Phase 2a, randomised, double-blind, placebo-controlled crossover study to explore the effects of ACD440 in patients with peripheral neuropathic pain with sensory hypersensitivity | |||||||||||||
Medical condition: Peripheral neuropathic pain with sensory hypersensitivity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002224-32 | Sponsor Protocol Number: SYNCHRO | Start Date*: 2019-11-12 | |||||||||||
Sponsor Name:Fundació Hospital Universitari Vall d' Hebrón - Institut de Recerca (VHIR) | |||||||||||||
Full Title: Sense, rhYhm & Networks: the study of how erenumab modulates CHROnic migraine | |||||||||||||
Medical condition: Chronic migraine | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004033-13 | Sponsor Protocol Number: EMA401-005 | Start Date*: 2012-02-06 | |||||||||||
Sponsor Name:Spinifex Pharmaceuticals Pty Ltd | |||||||||||||
Full Title: A Phase 2 open label biomarker study of angiotensin II type 2 receptor antagonist EMA401 for the treatment of pain in patients with chemotherapy-induced peripheral neuropathy. | |||||||||||||
Medical condition: Chemotherapy induced peripheral neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001371-24 | Sponsor Protocol Number: 6621 | Start Date*: 2019-01-08 |
Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
Full Title: Prospective, randomised, placebo-controlled study of polyvalent intravenous immunoglobulins for the treatment of primary Sjögren's syndrome associated painful sensory neuropathies | ||
Medical condition: Primary Sjögren's syndrome associated painful sensory neuropathies | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000838-12 | Sponsor Protocol Number: Vit-Caps-Protocol-V1.0 | Start Date*: 2006-08-03 |
Sponsor Name:Peter Wolf MD, Department of Dermatology, Medical University of Graz | ||
Full Title: Die Bedeutung des sensorischen Nervensystems für die Repigmentierung der Haut bei Vitiligo (engl.: The role of the sensory nervous system for repigmentation in vitiligo) | ||
Medical condition: Vitiligo | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000846-20 | Sponsor Protocol Number: ANE-INTRA-2013 | Start Date*: 2013-06-24 | |||||||||||
Sponsor Name:Fundació Parc Taulí | |||||||||||||
Full Title: Comparison of the effects of bupivacain or levobupivacain on cerebral oxigenation during intradural anesthesia in elderly patients who undergo major orthopaedic surgery for hip replacement | |||||||||||||
Medical condition: Intradural anaesthesia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006458-24 | Sponsor Protocol Number: V00116 TD 201 | Start Date*: 2008-01-23 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: Analysis of the sensory profile of two new transdermal patches (V0116TD07AF019 and V0116TD07AF020) 21 mg/24h versus a reference transdermal patch (NICOTINELL TTS) 21 mg/24h. | |||||||||||||
Medical condition: Healthy volunteers, occasional or regular smokers. Intended indication: Relief of nicotine withdrawal symptoms, in nicotine dependency as an aid to smoking cessation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003631-37 | Sponsor Protocol Number: UDC1 | Start Date*: 2017-01-24 |
Sponsor Name:Universitaire ziekenhuis Leuven | ||
Full Title: Therapeutic effect of ursodeoxycholic acid on duodenal permeability and meal related sensory motor function in functional dyspepsia patients | ||
Medical condition: Functional dyspepsia (FD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001285-11 | Sponsor Protocol Number: P20.XXX | Start Date*: 2021-01-12 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: A Randomized, open label, Non-inferiority trial on the efficacy of Lacosamide versus Duloxetine in Patients with Chemotherapy-induced Polyneuropathy – A strategy trial | ||
Medical condition: Chemotherapy-induced polyneuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-006235-33 | Sponsor Protocol Number: 738/02/2011 | Start Date*: 2012-03-30 | |||||||||||
Sponsor Name:MDM S.P.A. | |||||||||||||
Full Title: Sensory Motor Neuropathies of the sciatic nerve: a comparative evaluation of dextrorotatory enantiomer of thioctic acid and acetyl-L-carnitine. | |||||||||||||
Medical condition: sensitive motor sciatic neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
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: 2021-002810-15 | Sponsor Protocol Number: CHUB-Neuro-ENMG-MS | Start Date*: 2021-06-25 | |||||||||||
Sponsor Name:CHU Brugmann | |||||||||||||
Full Title: Peripheral neuropathy as potential side effect in patients with multiple sclerosis treated with teriflunomide. | |||||||||||||
Medical condition: Multiple sclerosis, treated with teriflunomide | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003172-36 | Sponsor Protocol Number: 29.06.2011 | Start Date*: 2011-10-07 | |||||||||||||||||||||
Sponsor Name:Department of Anaesthesia, Tampere University Hospital | |||||||||||||||||||||||
Full Title: Arousal reaction during desflurane anaesthesia | |||||||||||||||||||||||
Medical condition: The patients who undergo abdominal surgeries (laparotomy or laparoscopy) under desflurane anaesthesia will be investigated. | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000805-22 | Sponsor Protocol Number: A20175CI03 | Start Date*: 2021-09-28 |
Sponsor Name:Neuroplast BV | ||
Full Title: A multi-center, double-blind, randomized, placebo-controlled, delayed- start phase II/III study to assess the efficacy and safety of Neuro-Cells in (sub)acute spinal cord injury patients | ||
Medical condition: Traumatic Spinal cord injury | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005326-23 | Sponsor Protocol Number: PHRC-K2020PEZET | Start Date*: 2022-01-24 |
Sponsor Name:CHU de Clermont-Ferrand | ||
Full Title: Evaluation of the efficacy of donepezil in the treatment of oxaliplatin-induced peripheral neuropathy: proof of concept study | ||
Medical condition: Oxaliplatine-induced peripheral neuropathy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003684-54 | Sponsor Protocol Number: ACLS | Start Date*: 2014-03-27 |
Sponsor Name:Academic Medical Center Amsterdam | ||
Full Title: Analgesic efficacy of saphenous nerve blockade for outpatient knee anterior cruciate ligament surgery | ||
Medical condition: Mid thigh saphenous nerve block with levobupivacain, as compared to femoral nerve block, in patients undergoing anterior cruciate ligament surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000348-14 | Sponsor Protocol Number: NSTATIN | Start Date*: 2014-03-05 |
Sponsor Name:Odense University Hospital, Department of Neurology | ||
Full Title: Statin-treatment and peripheral neuropathy - a randomized clinical trial | ||
Medical condition: Patients with cerebral infarction or transient ischemic attack. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-000294-29 | Sponsor Protocol Number: PLD-Caps_Protocol-V1.0 | Start Date*: 2007-04-20 |
Sponsor Name:Department of Dermatology, medical University of Graz | ||
Full Title: Die Bedeutung des sensorischen Nervensystems der Haut bei polymorpher Lichtdermatose English title: The role of the cutaneous sensory nervous system in polymorphic light eruption (PLE) | ||
Medical condition: Polymorphic light eruption | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002223-28 | Sponsor Protocol Number: PHAO14-CH/TEPTAU | Start Date*: 2016-11-30 |
Sponsor Name:CHRU DE TOURS | ||
Full Title: Tau brain imaging in typical and atypical Alzheimer’s Disease (AD) | ||
Medical condition: Alzheimer's diseases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
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