- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
11 result(s) found for: Dissociation.
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EudraCT Number: 2016-000367-16 | Sponsor Protocol Number: 0305070106 | Start Date*: 2017-03-23 |
Sponsor Name:Radboud University Nijmegen | ||
Full Title: The effect of oxytocin administration on empathy and emotion recognition in healthy and antisocial adolescents | ||
Medical condition: We examine the effect of oxytocin administration on empathy and emotion recognition in healthy adolescents and adolescents with antisocial behavior and history of severe psychological trauma | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004090-28 | Sponsor Protocol Number: Fx-R-001-S1/B3461049 | Start Date*: 2014-05-13 |
Sponsor Name:Fold RX Pharmaceuticals, a Pfizer Company | ||
Full Title: TRANSTHYRETIN-ASSOCIATED AMYLOIDOSES OUTCOMES SURVEY (THAOS) – OPTIONAL BLOOD SAMPLE COLLECTION SUBSTUDY | ||
Medical condition: Transthyretin (TTR) a 127-amino acid, tetrameric protein, primarily synthesized in the liver, is a secreted protein present in the blood and cerebrospinal fluid and is a carrier of thyroxine and r... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-018486-37 | Sponsor Protocol Number: dexa2010 | Start Date*: 2010-05-21 |
Sponsor Name:Kris-och Traumacentrum | ||
Full Title: Treatment of exacerbations of post-traumatic stress disorder by short-term dexamethasone, a pilot study. | ||
Medical condition: Posttraumatic stress syndrome F431 | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000307-17 | Sponsor Protocol Number: 69HCL16_0743 | Start Date*: 2018-07-19 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Microcirculatory and Macrocirculatory Effects of Landiolol on Postoperative Atrial Fibrillation: a Randomized Study. MMELPOAF study. | |||||||||||||
Medical condition: Postoperative Atrial Fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001401-41 | Sponsor Protocol Number: TAPAS-2014 | Start Date*: 2014-07-29 |
Sponsor Name: | ||
Full Title: Targeting Antibiotics to Pseudomonas Aeruginosa in Small airways (TAPAS) study in patients with cystic fibrosis | ||
Medical condition: Cystic Fibrosis and chronic infection with Pseudomonas aeruginosa | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002718-17 | Sponsor Protocol Number: IMVT-1401-2401 | Start Date*: 2023-06-19 | |||||||||||
Sponsor Name:Immunovant Sciences, GmbH | |||||||||||||
Full Title: A Phase 2b, Multi-center, Randomized, Quadruple-blind, Placebo-controlled Study of Batoclimab Treatment in Adult Participants with Active Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | |||||||||||||
Medical condition: Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) NO (Trial now transitioned) BE (Trial now transitioned) FI (Trial now transitioned) SE (Trial now transitioned) DK (Trial now transitioned) SK (Trial now transitioned) PT (Trial now transitioned) BG (Trial now transitioned) ES (Ongoing) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002337-20 | Sponsor Protocol Number: 2412325-2 | Start Date*: 2006-09-06 | |||||||||||
Sponsor Name:Erasmus Medical Centre Rotterdam | |||||||||||||
Full Title: Efficacy of peripherally targeted inhaled rhDNase for persistent obstructive asthma in childhood | |||||||||||||
Medical condition: Asthma is a chronic inflammatory disorder in which many cells play a role, in particular mast cells, eosinophils and T lymphocytes. In susceptible individuals this inflammation causes recurrent epi... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004729-27 | Sponsor Protocol Number: 0504270672 | Start Date*: 2006-09-04 | |||||||||||
Sponsor Name:Organisation name was not entered | |||||||||||||
Full Title: Vähentääkö pintapuudutus karsastusleikkauksen aikaista nosiseptiivistä stressivastetta nukutetuilla lapsipotilailla | |||||||||||||
Medical condition: karsastusleikkaus | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003984-24 | Sponsor Protocol Number: EPIsoDE_01 | Start Date*: 2020-11-17 |
Sponsor Name:Central Institute of Mental Health | ||
Full Title: A phase II randomized, double-blind, active placebo-controlled parallel group trial to examine the efficacy and safety of psilocybin in treatment-resistant major depression | ||
Medical condition: Treatment-Resistant Depressive Episode or Treatment-Resistant Recurrent Depressive Disorder of moderate to severe degree withoutpsychotic features | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023782-22 | Sponsor Protocol Number: A9391010 | Start Date*: 2011-12-16 | |||||||||||
Sponsor Name:Pfizer, S.L.U. | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE-BLIND ASSESSMENT OF EFFICACY AND SAFETY OF PF-04171327(1, 5, 10, 15 MG DOSE, DAILY) COMPARED TO 5 MG AND 10 MG PREDNISONE DAILY AND PLACEBO DAILY IN SUBJECTS WITH RHEU... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) DE (Completed) HU (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004376-11 | Sponsor Protocol Number: AZM-MD-302 | Start Date*: 2012-05-15 | |||||||||||
Sponsor Name:Forest Research Institute, Inc. | |||||||||||||
Full Title: A Phase 3 Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study of the Effects of Once-Daily Oral Doses of 75 mg Azimilide Dihydrochloride on the Incidence of Cardiovascular Hospitalizat... | |||||||||||||
Medical condition: Ventricular arrhythmia in patients with implantable cardioverter-defibrillator (ICD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) NL (Prematurely Ended) ES (Prematurely Ended) DE (Prematurely Ended) SE (Prematurely Ended) CZ (Prematurely Ended) DK (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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