- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
4 result(s) found for: Visual Hallucination.
Displaying page 1 of 1.
EudraCT Number: 2008-006278-13 | Sponsor Protocol Number: NL24092.042.08 | Start Date*: 2009-02-04 | ||||||||||||||||
Sponsor Name:UMCG | ||||||||||||||||||
Full Title: Motor function optimization in advanced Parkinson’s disease patients, combined with galantamine to prevent visual hallucinations. | ||||||||||||||||||
Medical condition: patients with advanced (>5 years) Parkinson's disease and visual hallucinations. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024265-40 | Sponsor Protocol Number: KETA-FAN | Start Date*: 2011-10-27 | |||||||||||
Sponsor Name:HOSPITAL UNIVERSITARI DE BELLVITGE | |||||||||||||
Full Title: Perineural vs systemic N-methyl-D-aspartate (NMDA) receptors antagonism with ketamine as a reverser of peripheral and central sensitization in phantom limb pain | |||||||||||||
Medical condition: Phantom limb pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003623-37 | Sponsor Protocol Number: CAN-PDP | Start Date*: 2020-02-12 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: CANnabidiol for Parkinson’s Disease Psychosis | |||||||||||||
Medical condition: Parkinson's disease psychosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000149-34 | Sponsor Protocol Number: CR845-310302 | Start Date*: 2023-01-17 | |||||||||||
Sponsor Name:Cara Therapeutics, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled 12-Week Study to Evaluate the Safety and Efficacy of Oral Difelikefalin in Advanced Chronic Kidney Disease Subjects with Moderate-to-Seve... | |||||||||||||
Medical condition: Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) PL (Prematurely Ended) BG (Completed) | |||||||||||||
Trial results: (No results available) |
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