- Trials with a EudraCT protocol (80)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
80 result(s) found for: At risk mental state.
Displaying page 1 of 4.
EudraCT Number: 2020-000576-38 | Sponsor Protocol Number: CARL | Start Date*: 2022-06-08 | |||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI CAMERINO | |||||||||||||
Full Title: Effect of treatment of the cholinergic precursor Choline Alfoscerate in mild cognitive dysfunction | |||||||||||||
Medical condition: Mild cognitive dysfunction | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003076-22 | Sponsor Protocol Number: PSY-201401_ESPRIT | Start Date*: 2016-07-07 | ||||||||||||||||
Sponsor Name:Central Institute of Mental Health Mannheim (ZI) | ||||||||||||||||||
Full Title: Multimodal Prevention of First Psychotic Episode – a 2x2-Factorial Randomized Trial investigating the efficacy of Acetylcysteine (ACC) and Integrated Preventive Psychological Intervention (IPPI) in... | ||||||||||||||||||
Medical condition: Clinical High Risk state for developing a first psychotic episode | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021044-17 | Sponsor Protocol Number: CLOCK_depression | Start Date*: 2010-08-11 | |||||||||||
Sponsor Name:Medizinische Universität Wien | |||||||||||||
Full Title: The effect of agomelatine on CLOCK gene expression in patients with major depressive disorder and healthy controls: an exploratory study. | |||||||||||||
Medical condition: Major depressive disorder (MDD), Seasonal affective disorder (subtype of MDD) | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013069-24 | Sponsor Protocol Number: CRC/2008/03 | Start Date*: 2010-02-04 |
Sponsor Name:AZIENDA OSPEDALIERA - CENTRO RICERCHE CLINICHE DI VERONA | ||
Full Title: A double blind, single dose, randomized, 2-way crossover, placebo controlled study to set-up the resting state test in 10 healthy subjects | ||
Medical condition: NA, Set-up model study | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005004-13 | Sponsor Protocol Number: NEURAPRO-E FINAL Protocol | Start Date*: 2010-10-14 |
Sponsor Name:Orygen Research Centre | ||
Full Title: Add-on Therapie mit Omega-3 Fettsäuren bei Jugendlichen mit hohem Risiko für Schizophrenie und andere psychotische Störungen: eine Multizentren- Replikationsstudie Omega-3 Fatty Acids for Symptomat... | ||
Medical condition: In view of recent data and after a careful review of potentially neuroprotective treatment options in early psychotic illness, we have decided to replicate the findings of a randomized controlled t... | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001573-28 | Sponsor Protocol Number: Uni-Koeln-320 | Start Date*: 2007-11-26 |
Sponsor Name:Universität zu Köln | ||
Full Title: Prevent: Secondary Prevention of Schizophrenia. A randomized controlled trial. | ||
Medical condition: Persons at risk of being prodromally symptomatic of psychosis (PAR) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002386-18 | Sponsor Protocol Number: 11-185/CAIAC | Start Date*: 2016-03-15 |
Sponsor Name:RWTH Aachen Clinical Trials Center Aachen (CTC-A) | ||
Full Title: Network connectivity and inhibitory control under atomoxetin challenge - A pharamacological "resting state" and "inhibitory task" fMRI study in patients with ADHD | ||
Medical condition: Patients with Attention-Deficit/Hyperactivity Disorders (ADHD) | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-000121-31 | Sponsor Protocol Number: PSYK-TREAT-HEALTHY | Start Date*: 2013-03-20 | |||||||||||
Sponsor Name:Prof., dr. med. Anders Fink-Jensen | |||||||||||||
Full Title: Does a GLP-1 receptor agonist change glucose tolerance in antipsychotic-treated patients? | |||||||||||||
Medical condition: Dysglycaemia, schizophrenia, paranoid psycosis, schizotypal disorder | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005891-28 | Sponsor Protocol Number: CORICA | Start Date*: 2008-10-04 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Perspective evaluation on the role practiced by three different contraceptive hormonal on l I risk cardiovascular in young women: impact on the sensibility' insulinica | |||||||||||||
Medical condition: GIOVANI DONNE TRA 18 E 35 ANNI | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003866-14 | Sponsor Protocol Number: B5091007 | Start Date*: 2017-06-15 | ||||||||||||||||
Sponsor Name:Pfizer Inc. | ||||||||||||||||||
Full Title: A Phase 3, Placebo-Controlled, Randomized, Observer-Blinded Study To Evaluate The Efficacy, Safety, And Tolerability Of A Clostridium Difficile Vaccine In Adults 50 Years Of Age And Older | ||||||||||||||||||
Medical condition: Primary C difficile infection (CDI) | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) BG (Completed) SE (Completed) HU (Completed) BE (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) DE (Completed) FI (Completed) PT (Completed) ES (Completed) PL (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001056-17 | Sponsor Protocol Number: 3606 | Start Date*: 2020-08-14 | ||||||||||||||||
Sponsor Name:Kings's College London [...] | ||||||||||||||||||
Full Title: A randomised feasibility trial investigating Sativex® for the treatment of the Agitation & Aggression (A/A) in Alzheimer’s Dementia. | ||||||||||||||||||
Medical condition: Clinically significant agitation in Alzheimer's Diseases | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002787-32 | Sponsor Protocol Number: RG_19-172 | Start Date*: 2020-11-16 |
Sponsor Name:University of Birmingham | ||
Full Title: Antidepressant for the prevention of DEPression following first episode Psychosis trial | ||
Medical condition: Patients with First Episode Psychosis. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001249-41 | Sponsor Protocol Number: KEK-ZH-2012-0249 | Start Date*: 2013-04-12 |
Sponsor Name:University Hospital of Zurich and City Hospital Waid | ||
Full Title: Vitamin D3 – Omega3 – Home Exercise – HeALTHy Ageing and Longevity Trial Randomized, double-blind, placebo-controlled, multi-centre clinical trial | ||
Medical condition: healthy ageing, functional decline | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) PT (Completed) FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002187-22 | Sponsor Protocol Number: 001 | Start Date*: 2005-04-05 |
Sponsor Name:Ullevål University Hospital | ||
Full Title: Scandinavian Candesartan Acute Stroke Trial | ||
Medical condition: Acute stroke (ischemic or haemoragic) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) DK (Completed) BE (Completed) EE (Prematurely Ended) LT (Prematurely Ended) DE (Prematurely Ended) FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000001-23 | Sponsor Protocol Number: 14861B | Start Date*: 2014-02-27 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: An open-label extension study to evaluate the long-term safety and tolerability of Lu AE58054 as adjunctive treatment to donepezil in patients with mild-moderate Alzheimer's disease | |||||||||||||
Medical condition: Alzheimer´s disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) EE (Completed) IT (Completed) BE (Completed) LT (Completed) ES (Completed) DK (Completed) BG (Completed) PT (Completed) GB (Completed) HU (Completed) FI (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001542-38 | Sponsor Protocol Number: ANVS-22001 | Start Date*: 2023-01-09 |
Sponsor Name:Annovis Bio, Inc. | ||
Full Title: A 6-month prospective, randomized, double-blind, placebo-controlled clinical trial investigating the efficacy, safety, and tolerability of two different doses of buntanetap or placebo in patients w... | ||
Medical condition: Parkinson’s disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) HU (Completed) IT (Completed) PL (Completed) ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004762-15 | Sponsor Protocol Number: VUMC38027 | Start Date*: 2012-08-22 |
Sponsor Name:VU Univeristy Medical Centre | ||
Full Title: Early pharmacological intervention to prevent delirium: HAlopeRidol PrOphylaxis in Older emergency department patieNts. The HARPOON study | ||
Medical condition: Delirium | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001557-27 | Sponsor Protocol Number: B1931030 | Start Date*: 2019-02-17 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 4, OPEN-LABEL, RANDOMIZED STUDY OF TWO INOTUZUMAB OZOGAMICIN DOSE LEVELS IN ADULT PATIENTS WITH RELAPSED OR REFRACTORY B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA ELIGIBLE FOR HEMATOPOIETIC STEM CE... | |||||||||||||
Medical condition: ADULT PATIENTS WITH RELAPSED OR REFRACTORY B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA ELIGIBLE FOR HEMATOPOIETIC STEM CELL TRANSPLANTATION AND WHO HAVE RISK FACTOR(S) FOR VENO-OCCLUSIVE DISEASE | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) BE (Completed) HU (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002520-82 | Sponsor Protocol Number: CLO-MEAS | Start Date*: 2015-08-27 | |||||||||||
Sponsor Name:Prof., dr. med. Anders Fink-Jensen | |||||||||||||
Full Title: The significance of deviation in time from the 12-hour standard serum-clozapine monitoring | |||||||||||||
Medical condition: Treatment-resistant schizophrenia | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002226-23 | Sponsor Protocol Number: 2013-002226-23 | Start Date*: Information not available in EudraCT |
Sponsor Name:University of Bergen, Department of Global Public Health and Primary Care | ||
Full Title: Efficacy of Pain Treatment on Depression in Patients with Dementia. A Randomized Clinical Trial of Efficacy | ||
Medical condition: Depression Pain Dementia | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
