- Trials with a EudraCT protocol (37)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
37 result(s) found for: Geriatric Depression Scale.
Displaying page 1 of 2.
EudraCT Number: 2021-003437-10 | Sponsor Protocol Number: CARTESIO | Start Date*: 2023-04-05 | |||||||||||
Sponsor Name:Azienda Socio Sanitaria Territoriale di Lodi | |||||||||||||
Full Title: PILOT STUDY ON THE EFFECTIVENESS OF CHOLINE ALFOSCERATE IN THE UNDER THRESHOLD DEPRESSION OF THE ELDERLY | |||||||||||||
Medical condition: Under threshold depression of the elderly. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002411-27 | Sponsor Protocol Number: 2006-002411-27 | Start Date*: 2006-10-24 |
Sponsor Name:Universitair Psychiatrisch Centrum KU Leuven | ||
Full Title: Evaluation of the effect of escitalopram on cognitive and fine motor function in depressed elderly patients. | ||
Medical condition: Elderly depressed patients, MDD, DSM IV-TR, single episode or recurrent | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001622-26 | Sponsor Protocol Number: QQ05.16.02 | Start Date*: 2018-08-14 | |||||||||||
Sponsor Name:FIDIA FARMACEUTICI S.P.A. | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter clinical trial to assess safety and effectiveness of Liposom in enhance and speed up response to antidepressant therapy with citalopram i... | |||||||||||||
Medical condition: Major Depressive Disorder (MDD) in elderly patients | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000356-18 | Sponsor Protocol Number: 25051974 | Start Date*: 2023-12-21 |
Sponsor Name:Stichting Apotheek der Haarlemse Ziekenhuizen | ||
Full Title: Effect of repeated intranasal cobalamin administration on cobalamin deficiency in elderly | ||
Medical condition: Cobalamin (vitamin B12) deficiency | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004160-22 | Sponsor Protocol Number: LUMC_IEMO80PLUS_1.0 | Start Date*: 2013-06-18 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: IEMO 80-plus thyroid trial | ||
Medical condition: Subclinical hypothyroidism | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000219-15 | Sponsor Protocol Number: 13-10 | Start Date*: 2014-11-27 |
Sponsor Name:VU Medical Center | ||
Full Title: Amyloid pathology in cognitively normal elderly subjects | ||
Medical condition: Cognitively healthy elderly, aged 60-100 years old. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005218-13 | Sponsor Protocol Number: 2167SR | Start Date*: 2012-04-23 | ||||||||||||||||
Sponsor Name:Kings College London [...] | ||||||||||||||||||
Full Title: Rationalisation of antipsychotic drug use in older people, using [18F]-Fallypride PET | ||||||||||||||||||
Medical condition: Alzheimer's Disease and schizophrenia like illness | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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 |
EudraCT Number: 2005-003788-22 | Sponsor Protocol Number: 248.596 | Start Date*: 2006-01-06 |
Sponsor Name:Boehringer Ingelheim Limited | ||
Full Title: A randomized, double-blind, placebo-controlled, parallel group, efficacy study of pramipexole and placebo administered orally over a 12-week treatment phase in Parkinson’s disease patients with sta... | ||
Medical condition: A randomized, double-blind, placebo-controlled, parallel group, efficacy study of pramipexole and placebo administered orally over a 12-week treatment phase in Parkinson’s disease patients with sta... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) FI (Completed) SE (Completed) ES (Completed) AT (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003740-23 | Sponsor Protocol Number: AB13004 | Start Date*: 2015-02-04 | |||||||||||
Sponsor Name:AB Science | |||||||||||||
Full Title: A prospective, multicentre, randomised, double-blind, placebo-controlled, parallel groups, phase 2b/3 study to compare the efficacy and safety of masitinib versus placebo in the treatment of patien... | |||||||||||||
Medical condition: Progressive Supranuclear Palsy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001850-13 | Sponsor Protocol Number: GLP-1/MCI | Start Date*: 2015-09-11 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA DI PARMA | |||||||||||||
Full Title: Long-acting exenatide: a tool to stop cognitive decline in patients with mild cognitive impairment with or without dysglycemia? | |||||||||||||
Medical condition: Moderate cognitive impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004187-30 | Sponsor Protocol Number: CO17730 | Start Date*: 2011-12-14 | |||||||||||
Sponsor Name:Avraham Pharmaceuticals Ltd. | |||||||||||||
Full Title: A 36-month, multi-centre, randomized double-blind placebo-controlled study to evaluate the safety and efficacy of low dose Ladostigil in patients with Mild Cognitive Impairment (MCI) | |||||||||||||
Medical condition: Patient with Mild Cognitive Impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004802-70 | Sponsor Protocol Number: APHP200491 | Start Date*: 2021-08-03 |
Sponsor Name:Assistance Publique – Hôpitaux de Paris | ||
Full Title: Impact of post-ARDS COVID sedation on late neuroinflammation | ||
Medical condition: All patients who have developed and survived ARDS linked to COVID-19 infection, admitted to intensive care units, meeting the study's inclusion criteria may be included in this research. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002715-15 | Sponsor Protocol Number: CAPI015A2201J | Start Date*: 2016-06-13 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, two-cohort parallel group study to evaluate the efficacy of CAD106 and CNP520 in participants at risk for the onset of clinical symptoms of Alzheimer... | |||||||||||||
Medical condition: Alzheimer's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Prematurely Ended) FI (Prematurely Ended) NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002654-75 | Sponsor Protocol Number: EVP-6124-026 | Start Date*: 2015-08-04 | ||||||||||||||||
Sponsor Name:Forum Pharmaceuticals Inc. | ||||||||||||||||||
Full Title: A 26-Week Extension Study of the Safety and Clinical Effects of EVP-6124 in Subjects with Alzheimer’s Disease Currently or Previously Receiving an Acetylcholinesterase Inhibitor Medication | ||||||||||||||||||
Medical condition: Alzheimer’s Disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) NL (Completed) CZ (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000823-15 | Sponsor Protocol Number: NEUPRODEX | Start Date*: 2013-12-23 |
Sponsor Name:Charité – Universitätsmedizin Berlin | ||
Full Title: Neuroprotection with Dexmedetomidine in patients undergoing elective cardiac or abdominal surgery | ||
Medical condition: The drug Dexmedetomidine will be investigated in patients (men and women) undergoing elective cardiac or abdominal surgery. The study medication will be administered perioperatively by intravenous ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001720-35 | Sponsor Protocol Number: P/2018/395 | Start Date*: 2019-05-29 |
Sponsor Name:CHU de Besançon | ||
Full Title: Evaluation de l’intérêt d’une polychimiothérapie par XELOXIRI-3 chez les patients âgés ou fragiles atteints d’un adénocarcinome pancréatique métastatique | ||
Medical condition: cancers du pancréas | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004865-26 | Sponsor Protocol Number: M12-927 | Start Date*: 2015-08-27 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: An Open-label, Randomized 26-Week Study Comparing Levodopa-Carbidopa INteStInal Gel (LCIG) Therapy to Optimized Medical Treatment (OMT) on Non-Motor Symptoms (NMS) in Subjects with Advanced Parkins... | |||||||||||||
Medical condition: Non-motor symptoms in advanced Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) SE (Completed) IT (Completed) ES (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023322-21 | Sponsor Protocol Number: NP031112-10B04 | Start Date*: 2011-04-13 | |||||||||||
Sponsor Name:Noscira S.A | |||||||||||||
Full Title: A multicenter, Randomized, Double-blind, Placebo-controlled, 4-arm, 26 week Parallel-Group Study to evaluate the Efficacy, Safety and Tolerability of Two Oral Doses and Two Regimes of Tideglusib vs... | |||||||||||||
Medical condition: Alzheimer's Disease (mild to moderate) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) FI (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000604-15 | Sponsor Protocol Number: PTC-19-602325 | Start Date*: 2020-10-29 | |||||||||||
Sponsor Name:UNIVERSITÀ DEGLI STUDI "G. D'ANNUNZIO" CHIETI-PESCARA | |||||||||||||
Full Title: Multicentre, randomized, double-blind, placebo-controlled, parallel-group Phase II study aimed at evaluating the efficacy and safety of “Zinco Solfato” in Mild Cognitive Impairment due to Alzheimer... | |||||||||||||
Medical condition: Prodromic Alzheimer's disease with evidence of cerebral amyloidosis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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