- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: Neurons.
Displaying page 1 of 2.
EudraCT Number: 2018-002192-18 | Sponsor Protocol Number: PrucaloprideRNAseq | Start Date*: 2018-09-14 |
Sponsor Name:KU Leuven | ||
Full Title: Characterization of nerve-modulated macrophage population in the gastrointestinal tract | ||
Medical condition: Patients undergoing colorectal surgery due to benign or malignant carcinoma, diverticulitis or constipation drug will be used to differentiate between macrophages that are modulated by enteric neu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003001-94 | Sponsor Protocol Number: MSGLP | Start Date*: 2019-11-06 | |||||||||||
Sponsor Name:Lekárska fakulta UK Bratislava | |||||||||||||
Full Title: Use of GLP-1 analogs in the treatment of multiple sclerosis | |||||||||||||
Medical condition: Our hypothesis is that patients with MS have a disorder of energy metabolism in neurons and glial cells of the CNS, contributing to the development and progression of demyelinating foci and neurode... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002228-28 | Sponsor Protocol Number: STEMALS-II | Start Date*: 2014-09-01 |
Sponsor Name:Università degli Studi di Torino e Azienda Ospedaliera Città della Salute e della Scienza di Torino | ||
Full Title: A double blind, placebo controlled, parallel groups, multicenter study on filgrastim in amyotrophic lateral sclerosis | ||
Medical condition: Amyotrophic lateral sclerosis (ALS) is a severe progressive neurological disorder characterized by a selective degeneration of spinal, bulbar, and cortical motor neurons. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018233-21 | Sponsor Protocol Number: WEC 0910 | Start Date*: 2010-03-31 |
Sponsor Name:Leiden University Medical Centre | ||
Full Title: Modeling the respiratory effects of subanesthetic doses of propofol under closed-loop or non-steady-state conditions without and with a remifentanil background infusion in healthy volunteers. | ||
Medical condition: This study is performed in healthy volunteers. The study is aimed at investigating the effect of propofol and remifentanil-propofol interaction on breathing in awake, non-artificially ventilated vo... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000142-18 | Sponsor Protocol Number: 1.0 | Start Date*: 2018-05-09 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Feasibility and pharmacodynamics of subcutaneously given combination of dexmedetomidine and ketamine infusion in ALS patients receiving palliative care | |||||||||||||
Medical condition: Amyotrophic lateral sclerosis (ALS) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000934-19 | Sponsor Protocol Number: 2005-130 | Start Date*: 2005-05-19 |
Sponsor Name:Neurologisk Afdeling Århus Universitetshospital | ||
Full Title: Undersøgelse af subcutan immunglobulin behandling af patienter med multifokal motorisk neuropati | ||
Medical condition: Multifokal motor neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002099-15 | Sponsor Protocol Number: APOCT-001 | Start Date*: 2014-09-15 | |||||||||||
Sponsor Name:Apodemus AB | |||||||||||||
Full Title: A randomised, double blind, placebo controlled trial to evaluate the safety and efficacy of Apovir for treatment of patients with Amyotrophic lateral sclerosis | |||||||||||||
Medical condition: Amyotrophic Lateral Sclerosis (ALS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001202-14 | Sponsor Protocol Number: CiPA001 | Start Date*: 2019-06-05 |
Sponsor Name:Amsterdam UMC | ||
Full Title: CiPA Trial: Effect of Citalopram on chest pain in patients with achalasia | ||
Medical condition: Achalasia is a motility disorder of the esophagus. Disappearance of myenteric neurons in the esophageal wall leads to failure of relaxation of the lower esophageal sphincter (LES) and impaired peri... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000247-27 | Sponsor Protocol Number: ZX-2018-LBT999-DATTEP-3 | Start Date*: 2021-03-31 | ||||||||||||||||
Sponsor Name:ZIONEXA | ||||||||||||||||||
Full Title: Non-inferiority study of the molecular imaging of dopamine transporters using [123I]-FP/CIT-SPECT and [18F] LBT-999-PET to distinguish between Parkinson’s Disease and Essential Tremor. | ||||||||||||||||||
Medical condition: Patients suffering from an essential tremor or with Parkinson's disease. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003556-31 | Sponsor Protocol Number: SHP-607-201 | Start Date*: 2015-02-10 |
Sponsor Name:Premacure AB, A Member of the Shire Group of Companies | ||
Full Title: Long-term Outcome of Children Enrolled in Study ROPP-2008-01 Previously Treated with rhIGF-1/rhIGFBP-3 for the Prevention of Retinopathy of Prematurity (ROP) or Who Received Standard Neonatal Care | ||
Medical condition: Retinopathy of Prematurity (ROP) | ||
Disease: | ||
Population Age: Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) NL (Completed) PL (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-000491-18 | Sponsor Protocol Number: AT-007-1005 | Start Date*: 2022-09-14 | |||||||||||
Sponsor Name:Applied Therapeutics Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Two-Part Study to Evaluate the Pharmacodynamic Efficacy and Clinical Benefit of AT 007 in Patients with Sorbitol Dehydrogenase (SORD) Deficiency | |||||||||||||
Medical condition: SoRbitol Dehydrogenase (SORD) DEficiency | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005367-32 | Sponsor Protocol Number: PROMISE | Start Date*: 2016-02-29 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS ISTITUTO NEUROLOGICO CARLO BESTA | |||||||||||||
Full Title: PROTEIN MISFOLDING, AMYOTROPHIC LATERAL SCLEROSIS AND GUANABENZ: A PHASE II RCT WITH FUTILITY DESIGN | |||||||||||||
Medical condition: Amiotrophic Lateral Sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000431-22 | Sponsor Protocol Number: CLLLN | Start Date*: 2005-03-10 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: VALUTATION OF PLACEBO EFFECT AFTER CONDITIONING WITH APOMORPHINE AND WITHOUT PHARMACOLOGICAL CONDITIONING ON THE RIGIDITY AND ELECTRICAL ACTIVITY OF NEURONS OF SUBTHALAMIC NUCLEUS IN PARKINSON PATI... | |||||||||||||
Medical condition: THE TOPICAL INVESTIGATION IS THE BASE OF PATOLOGY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002968-27 | Sponsor Protocol Number: CFTY720D2402 | Start Date*: 2013-01-29 | |||||||||||
Sponsor Name:Novartis Farmaceutica, S.A | |||||||||||||
Full Title: A 48-week, double-blind, randomized, multi-center, parallelgroup study comparing structural changes in the retina and evolution of visual function after immediate versus delayed treatment with fing... | |||||||||||||
Medical condition: acute demyelinating optic neuritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Prematurely Ended) GB (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005182-31 | Sponsor Protocol Number: RCCSCAN | Start Date*: 2017-02-23 | |||||||||||
Sponsor Name:Lund University | |||||||||||||
Full Title: "An exploratory study regarding the use of the biomarker DAT for image diagnosis of clear cell renal cell carcinoma" | |||||||||||||
Medical condition: Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007320-25 | Sponsor Protocol Number: TRO19622 CL E Q 1015-1 | Start Date*: 2009-06-24 | |||||||||||
Sponsor Name:TROPHOS SA | |||||||||||||
Full Title: Phase II/III, multicenter, randomized, parallel group,double-blind, placebo controlled study to assess safety and efficacy of TRO19622 in Amyotrophic Lateral Sclerosis (ALS) patients treated with r... | |||||||||||||
Medical condition: ALS is a fatal neuromuscular disorder causing progressive loss of nervous control of voluntary muscles because of destruction of motor neurons in the brain and spinal cord.Riluzole is the only appr... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) GB (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003370-27 | Sponsor Protocol Number: DMFMRI201303 | Start Date*: 2014-09-25 |
Sponsor Name:Rainer Rupprecht, Klinik und Poliklinik für Psychiatrie und Psychotherapie der Universität Regensburg am Bezirksklinikum | ||
Full Title: Functional MRI (fMRI) after challenge and treatment with antidepressants and their relation to the clinical course, to the Hypothalamus-Hypophysis-Adrenocortical Axis and the colon microbiome | ||
Medical condition: Major Depressive Disorder is a chronic stress related disorder characterized by depressed mood and by vegetative and cognitive symptoms. Moreover, genetic, neuroendocrine and neurochemical biomarke... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002110-22 | Sponsor Protocol Number: LTA-2-2008 | Start Date*: 2008-09-16 | |||||||||||
Sponsor Name:Prof. dr L.H. van den Berg, UMC-Utrecht | |||||||||||||
Full Title: A randomised sequential trial of Lithium in amyotrophic lateral sclerosis | |||||||||||||
Medical condition: Amyotrophic lateral sclerosis (ALS) is a disease characterised by progressive degeneration of motor neurons in brain and spinal cord leading to muscle weakness. ALS can occur at anytime in adulthoo... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003265-19 | Sponsor Protocol Number: PD0053 | Start Date*: 2021-06-07 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: A Double-Blind, Placebo-Controlled, Randomized, 18-Month Phase 2a Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of Oral UCB0599 in Study Participants With Early Parkins... | |||||||||||||
Medical condition: Early-stage Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) FR (Ongoing) PL (Ongoing) ES (Ongoing) NL (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000826-22 | Sponsor Protocol Number: CBLZ945C12201 | Start Date*: 2019-09-17 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: An open-label, adaptive design study in patients with amyotrophic lateral sclerosis (ALS) to characterize safety, tolerability and brain microglia response, as measured by TSPO binding, following m... | |||||||||||||
Medical condition: Amyotrophic lateral sclerosis (ALS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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