- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Synapse.
Displaying page 1 of 1.
| EudraCT Number: 2019-000617-37 | Sponsor Protocol Number: NL68690.091.18 | Start Date*: 2019-07-11 |
| Sponsor Name:Rijnstate ziekenhuis | ||
| Full Title: StudY of effect of Nimodipine and Acetaminophen on Postictal Symptoms after ECT | ||
| Medical condition: Postictal phenomena after electroconvulsive therapy (ECT) induced seizures. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-002511-22 | Sponsor Protocol Number: 20-05 | Start Date*: 2023-06-08 |
| Sponsor Name:Amsterdam UMC VUmc | ||
| Full Title: Synaptic density and tau pathology in Alzheimer's disease | ||
| Medical condition: Amyloid-beta positive individuals across the Alzheimer's disease continuum | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-004005-11 | Sponsor Protocol Number: ESKETINTRD2003 | Start Date*: 2013-12-17 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Double-Blind, Doubly-Randomized, Placebo-Controlled Study of Intranasal Esketamine in an Adaptive Treatment Protocol to Assess Safety and Efficacy in Treatment-Resistant Depression (SYNAPSE) | |||||||||||||
| Medical condition: Treatment Resistant Major Depression | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-002301-24 | Sponsor Protocol Number: NMD670-02-0001 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:NMD Pharma A/S | |||||||||||||
| Full Title: A Phase 2, randomised, double-blind, placebo-controlled, 2-way crossover study to evaluate the efficacy, safety, and tolerability of NMD670 in ambulatory adults with Type 3 spinal muscular atrophy | |||||||||||||
| Medical condition: Type 3 spinal muscular atrophy | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) BE (Trial now transitioned) DK (Trial now transitioned) DE (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004255-70 | Sponsor Protocol Number: 205687 | Start Date*: 2017-05-29 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A randomised, double-blind, parallel group PhIII study to assess the clinical efficacy and safety of 100 mg SC Mepolizumab as an add on to maintenance treatment in adults with severe bilateral nasa... | |||||||||||||
| Medical condition: Treatment of nasal polyposis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) SE (Completed) NL (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003392-32 | Sponsor Protocol Number: 2014/VCC/0014 | Start Date*: 2014-10-24 | |||||||||||
| Sponsor Name:Velindre NHS Trust | |||||||||||||
| Full Title: A Phase II/III trial of risk-stratified, reduced intensity adjuvant treatment in patients undergoing transoral surgery for Human papillomavirus (HPV)-positive oropharyngeal cancer | |||||||||||||
| Medical condition: Oropharyngeal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) DE (Trial now transitioned) ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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