- Trials with a EudraCT protocol (124)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
124 result(s) found for: Delirium.
Displaying page 1 of 7.
EudraCT Number: 2007-005300-41 | Sponsor Protocol Number: IC-DEL | Start Date*: 2008-05-27 | |||||||||||||||||||||||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||||||||||||||||||||||
Full Title: Rivastigmine for delirium in Intensive Care patients, a double-blind, randomised, placebo-controlled, multi-center add-on trial | |||||||||||||||||||||||||||||||||
Medical condition: Delirium | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002492-29 | Sponsor Protocol Number: 1928376455 | Start Date*: 2014-10-10 | |||||||||||||||||||||
Sponsor Name:Department of anaesthesia and intensive care, Hvidovre Hospital | |||||||||||||||||||||||
Full Title: The effect of Single-Dose Glucocorticoid on Postoperative delirium among Elderly Hip Fracture Patientes: A Randomized Placebo Controlled Study | |||||||||||||||||||||||
Medical condition: Postoperative Delirium | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003115-20 | Sponsor Protocol Number: 848041001 | Start Date*: 2018-02-19 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Erasmus Medical Center Rotterdam | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Efficacy of haloperidol to decrease the burden of delirium in adult critically ill patients: a prospective randomised multicenter double-blind placebo-controlled clinical trial | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Delirium | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001260-37 | Sponsor Protocol Number: PRODEO | Start Date*: 2017-05-23 | |||||||||||
Sponsor Name:Zuyderland Medical Center | |||||||||||||
Full Title: PRODEO: PROfylactic Haloperidol in patients defined as high risk for DElirium with delirium risk mOdel | |||||||||||||
Medical condition: Delirium | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000262-20 | Sponsor Protocol Number: DPOD III | Start Date*: 2007-07-25 | |||||||||||
Sponsor Name:Stanmore Clinical Research Facility Ltd | |||||||||||||
Full Title: A phase III, 7 days randomised, double-blind, placebo-controlled, parallel group study to assess efficacy of DPZ for reducing the symptoms of post-operative delirium after an elective hip or knee r... | |||||||||||||
Medical condition: Post-operative delirium. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006452-22 | Sponsor Protocol Number: maple b | Start Date*: 2009-04-01 | |||||||||||
Sponsor Name:Academic Medical Centre | |||||||||||||
Full Title: The effects of melatonin in the treatment of delirium | |||||||||||||
Medical condition: Delirium in elderly patients (65 yrs and older) acutely admitted to the ward of internal medicine. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003965-42 | Sponsor Protocol Number: 002 | Start Date*: 2007-12-04 | ||||||||||||||||
Sponsor Name:University Medical Centre Utrecht | ||||||||||||||||||
Full Title: Methylphenidate, rivastigmine or haloperidol in hypoactive delirious intensive care patients: a single centre, randomized, mono-blind pilot trial | ||||||||||||||||||
Medical condition: Hypoactive delirious ICU-patients | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000996-57 | Sponsor Protocol Number: MAPLE A | Start Date*: 2009-04-01 | |||||||||||
Sponsor Name:Academic Medical Centre | |||||||||||||
Full Title: The effects of melatonin the occurence of on post-operative delirium in hip fracture patients – a randomized double-blind placebo controlled trial | |||||||||||||
Medical condition: Delirium in elderly patients, acutely admitted for hip-fracture. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003547-39 | Sponsor Protocol Number: 46077 | Start Date*: 2013-10-15 | |||||||||||||||||||||||||||||||
Sponsor Name:Isala Klinieken | |||||||||||||||||||||||||||||||||
Full Title: Dexmedetomidine vs. clonidine in delirious intensive care patients: a randomised open-label trial | |||||||||||||||||||||||||||||||||
Medical condition: (ICU- associated) Delirium | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000815-26 | Sponsor Protocol Number: LUCID | Start Date*: 2013-08-26 |
Sponsor Name:Oslo University Hospital | ||
Full Title: THE OSLO STUDY OF CLONIDINE IN ELDERLY PATIENTS WITH DELIRIUM | ||
Medical condition: Delirium in elderly patients admitted to the acute geriatric ward | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005827-35 | Sponsor Protocol Number: RC31/20/0441 | Start Date*: 2021-03-25 |
Sponsor Name:University Hospital of Toulouse | ||
Full Title: SARS-CoV-2 neurotropism, micRoglial ActivatioN and cytokine dySregulaTiOn in COVID-19 patients with delirium | ||
Medical condition: delirium | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003829-15 | Sponsor Protocol Number: AID-ICU | Start Date*: 2017-11-30 |
Sponsor Name:Zealand University Hospital | ||
Full Title: Agents Intervening against Delirium in the Intensive Care Unit (AID-ICU) | ||
Medical condition: Treatment of delirium in critically ill adult patients in intensive care unit. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) FI (Completed) ES (Ongoing) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003321-14 | Sponsor Protocol Number: P160942J | Start Date*: 2018-08-03 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Prevention of DElirium with MELatonine in intensive care unit : prospective, multicenter, randomized, double-blind, placebo, multi-arm, multi-stage trial. | |||||||||||||
Medical condition: patients in intensive care unit with invasive mechanical ventilation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004434-32 | Sponsor Protocol Number: PREPOD | Start Date*: 2007-02-06 |
Sponsor Name:Technische Universität München, Fakultät für Medizin, Klinikum rechts der Isar | ||
Full Title: Prevention of postoperative delirium with donepezil | ||
Medical condition: Postoperative delirium | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006221-14 | Sponsor Protocol Number: AM-KS-III/06/08 | Start Date*: 2010-04-06 | |||||||||||
Sponsor Name:Company: Dr. Franz Köhler Chemie GmbH | |||||||||||||
Full Title: Wirksamkeit und Verträglichkeit von Physostigminsalicylat zur Behandlung des post-operativen Delirs nach Aorto-Koronarer-Bypass-Operation. Eine prospektive, doppelblinde, randomisierte, placebo... | |||||||||||||
Medical condition: Patients with postoperative delirium in the termination phase of anaesthesia after ACVB or aortic valve/mitral valve surgery or double heart intervention (heart-lung-machine (HLM) and mild hypother... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007384-17 | Sponsor Protocol Number: 3005099 | Start Date*: 2009-11-30 | ||||||||||||||||||||||||||
Sponsor Name:Sten Walther | ||||||||||||||||||||||||||||
Full Title: A prospective, multi-centre, randomised, double-blind, placebo-controlled comparison of intravenous dexmedetomidine with haloperidol in treatment of hyperactive delirium after heart surgery. | ||||||||||||||||||||||||||||
Medical condition: Postoperative hyperactive delirium | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004117-27 | Sponsor Protocol Number: QUEPRO | Start Date*: 2018-02-27 |
Sponsor Name:IBSAL (Instituto de Investigación Biomédica de | ||
Full Title: CONTROLLED, DOUBLE-BLIND, RANDOMIZED CLINICAL TRIAL FOR PROPHILAXIS OF POSOPERATIVE DELIRIUM IN HIGH RISK SURGICAL PATIENTS WITH QUETIAPINE. | ||
Medical condition: Postoperative delirium in high risk surgical patients. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-003114-13 | Sponsor Protocol Number: 1 | Start Date*: 2012-12-07 |
Sponsor Name:West Hertfordshire Hospitals NHS Trust | ||
Full Title: Hydroxymethylglutaryl-CoA reductase inhibition with simvastatin in mechanically ventilated patients at high risk of delirium | ||
Medical condition: Delirium | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-006464-24 | Sponsor Protocol Number: 20211125 | Start Date*: 2022-12-14 | |||||||||||
Sponsor Name:Rigshospitalet, Department of Anesthesiology, Juliane Marie Center | |||||||||||||
Full Title: Intravenous MELAtonin for prevention of Postoperative Agitation and Emergence Delirium in children. The MELA-PAED trial: a randomized, double-blind, placebo-controlled clinical trial. | |||||||||||||
Medical condition: Emergence delirium Postoperative agitation | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007237-47 | Sponsor Protocol Number: PHYDELIO | Start Date*: 2009-01-15 |
Sponsor Name:Charité - Universitätsmedizin Berlin | ||
Full Title: Perioperative physostigmine prophylaxis for liver resection patients at risk for delirium and postoperative cognitive dysfunction Perioperative Gabe von Physostigmin bei Leberteilresktion zur Prop... | ||
Medical condition: The drug physostigmine will be investigated in patients (men and women)undergoing a liver resection. The study medication will be administered by intravenous infusion continuously (24 hours) to pre... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
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