- Trials with a EudraCT protocol (160)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (9)
160 result(s) found for: Falls.
Displaying page 1 of 8.
EudraCT Number: 2013-001677-24 | Sponsor Protocol Number: 2012GR06 | Start Date*: 2013-06-20 |
Sponsor Name:University of Dundee [...] | ||
Full Title: Do ACE inhibitors reduce postural instability in older people?: Towards a novel approach to falls prevention. | ||
Medical condition: Falls in older people | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001411-12 | Sponsor Protocol Number: CBYM338B2203E1 | Start Date*: 2015-11-04 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: Extension of the CBYM338B2203 phase IIb/III study to evaluate the long-term efficacy, safety and tolerability of intravenous BYM338 in patients with sporadic inclusion body myositis | |||||||||||||
Medical condition: Sporadic Inclusion Body Myositis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) NL (Completed) DK (Completed) GB (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003684-54 | Sponsor Protocol Number: ACLS | Start Date*: 2014-03-27 |
Sponsor Name:Academic Medical Center Amsterdam | ||
Full Title: Analgesic efficacy of saphenous nerve blockade for outpatient knee anterior cruciate ligament surgery | ||
Medical condition: Mid thigh saphenous nerve block with levobupivacain, as compared to femoral nerve block, in patients undergoing anterior cruciate ligament surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002627-16 | Sponsor Protocol Number: IRL752C003 | Start Date*: 2022-07-28 | |||||||||||
Sponsor Name:Integrative Research Laboratories Sweden AB (IRLAB) | |||||||||||||
Full Title: A randomised, placebo-controlled, multicentre phase IIb study evaluating the efficacy of pirepemat on falls frequency in patients with Parkinson’s disease | |||||||||||||
Medical condition: Parkinson’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) FR (Completed) ES (Ongoing) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000047-33 | Sponsor Protocol Number: VitD-EX1.0 | Start Date*: 2014-03-20 |
Sponsor Name:VU University Medical Centre | ||
Full Title: The effect of high-resistance muscle strength training and vitamin D supplementation in persons with knee osteoarthritis | ||
Medical condition: knee osteoarthritis vitamin D deficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004903-33 | Sponsor Protocol Number: IBM4809 | Start Date*: 2018-06-18 | |||||||||||
Sponsor Name:Orphazyme A/S | |||||||||||||
Full Title: Phase 2/3 Study of Arimoclomol in Inclusion Body Myositis (IBM) A Randomized, Double-blind, Placebo-Controlled Trial | |||||||||||||
Medical condition: Sporadic Inclusion Body Myositis (sIBM) | |||||||||||||
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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: 2011-003053-25 | Sponsor Protocol Number: 1466 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:Research and Enterprise Department | |||||||||||||
Full Title: A randomised, double blind, placebo controlled trial to evaluate the effect of Rivastigmine on gait in people with Parkinson’s disease who have fallen. | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003934-14 | Sponsor Protocol Number: 86,1,2006_06_01 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Universitätsmedizin Göttingen | |||||||||||||
Full Title: „Eine randomisierte, placebokontrollierte Doppelblindstudie zur Evaluation der Effektivität oral verabreichten Doxycyclins bei Patienten mit Creutzfeldt-Jakob-Krankheit“ | |||||||||||||
Medical condition: Creutzfeldt-Jakob-Krankheit | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001153-17 | Sponsor Protocol Number: 262 | Start Date*: 2008-06-16 | |||||||||||
Sponsor Name:MSD | |||||||||||||
Full Title: Phase III (Phase V Program), Open-Label, Randomized, Referred- Care-Controlled, Clinical Trial to Evaluate the Efficacy and Safety of MK-0217A/Alendronate Sodium 70 mg/Vitamin D3 5600 I.U. Combinat... | |||||||||||||
Medical condition: Postmenopausal women with osteoporosis at increased risk of falls. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) ES (Completed) LT (Completed) GB (Completed) BE (Completed) LV (Completed) FR (Completed) IE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003219-23 | Sponsor Protocol Number: 2844 | Start Date*: 2019-06-28 | ||||||||||||||||
Sponsor Name:University of Bristol | ||||||||||||||||||
Full Title: CHIEF-PD (CHolinesterase Inhibitor to prEvent Falls in Parkinson’s Disease): A phase 3 randomised double-blind placebo-controlled trial of rivastigmine to prevent falls in Parkinson’s disease | ||||||||||||||||||
Medical condition: This trial will investigate the effectiveness of Rivastigmine on prevention of falls in patients with Parkinson's disease | ||||||||||||||||||
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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: 2009-011902-41 | Sponsor Protocol Number: TISOC-1 | Start Date*: 2009-08-05 |
Sponsor Name:Universitätsklinikum Jena, Friedrich-Schiller-Universität Jena | ||
Full Title: Split-dose TPF-Induction chemotherapy before Surgery of Oropharyngeal and cavity of the mouth Cancer | ||
Medical condition: Patienten mit einem histologisch nachgewiesenen, primär resektablen Plattenepithelcarcinoms des Oropharynx und der Mundhöhle | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003998-27 | Sponsor Protocol Number: RD-5103-003-06 | Start Date*: 2007-03-15 |
Sponsor Name:Derby Hospitals NHS Foundation Trust | ||
Full Title: Cardiovascular and functional consquences of chronic kidney disease in older people | ||
Medical condition: Chronic Kidney Disease Hypertension Falls | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-001778-40 | Sponsor Protocol Number: VITAMINA_D | Start Date*: 2017-10-11 |
Sponsor Name:Leonor Cuadra Llopart | ||
Full Title: A Prospective Randomized Trial Comparing the Effect of 2 vitamin D supplementation regimens in elderly people after hip fracture surgery | ||
Medical condition: Hip fracture and vitamin D deficiency | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022763-35 | Sponsor Protocol Number: VITAMINDHeartFailure1.0 | Start Date*: 2011-03-31 |
Sponsor Name:Medical University of Graz | ||
Full Title: Vitamin D supplementation in chronic heart failure: a randomized, double-blind, placebo-controlled trial | ||
Medical condition: Chronic stable heart failure (NYHA II-IV, ejection fraction ≤ 40%) Vitamin D deficiency (defined as 25 (OH) Vitamin D ≤ 30ng/ml) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004425-27 | Sponsor Protocol Number: 5863 | Start Date*: 2012-05-29 |
Sponsor Name:Newcastle Upon Tyne Hospitals NHS Foundation Trust | ||
Full Title: Study of Optimal Replacement of Thyroxine in the ElDerly (SORTED) SORTED 1 – a Randomised Controlled Trial (Pilot study) SORTED 2 – Qualitative Interviews SORTED 3 – Retrospective Cohort | ||
Medical condition: hypothyroidism (elderly individuals) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002425-30 | Sponsor Protocol Number: 0171 | Start Date*: 2020-03-17 |
Sponsor Name:Theravance Biopharma Ireland Limited | ||
Full Title: A Phase 3, 182-week, Open-Label, Extension Study to Investigate the Safety and Tolerability Study of TD-9855 in Treating Symptomatic Neurogenic Orthostatic Hypotension (symptomatic nOH) in Subjects... | ||
Medical condition: Symptomatic Neurogenic Orthostatic Hypotension in Subjects with Primary Autonomic Failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) ES (Prematurely Ended) PL (Completed) EE (Completed) FR (Completed) PT (Prematurely Ended) AT (Prematurely Ended) BG (Prematurely Ended) DE (Prematurely Ended) HU (Completed) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-004514-25 | Sponsor Protocol Number: SEDISTRESS | Start Date*: 2018-08-17 | ||||||||||||||||
Sponsor Name:Nutrición Medica S.L. | ||||||||||||||||||
Full Title: EFFICACY AND SAFETY OF THE ADMINISTRATION OF THE PASSIFLORA EXTRACT FOR BENZODIAZEPINE WITHDRAWAL IN INSTITUTIONALIZED OLDER ADULTS : CLINICAL TRIAL PHASE III. | ||||||||||||||||||
Medical condition: benzodiazepines withdrawn | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006964-48 | Sponsor Protocol Number: 20040215 | Start Date*: 2007-04-13 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: An Open-Label, Multi-Center, Phase 2 Safety and Efficacy Study of Denosumab (AMG 162) in Subjects with Recurrent or Unresectable Giant Cell Tumor (GCT) of Bone | |||||||||||||
Medical condition: Giant Cell Tumor (GCT) of bone | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001410-20 | Sponsor Protocol Number: NL81154.091.22 | Start Date*: 2022-09-21 |
Sponsor Name:Radboud university medical center | ||
Full Title: Determining the clinical relevance of the interaction between enzalutamide and the opioid morphine and the DOAC edoxaban to improve rational pharmacological care of patients with prostate cancer | ||
Medical condition: Prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002889-38 | Sponsor Protocol Number: OV-WV03 | Start Date*: 2004-12-16 |
Sponsor Name:OmniVision GmbH | ||
Full Title: Randomisierte, kontrollierte, doppelblinde klinische Prüfung zur Untersuchung der Wirksamkeit und Verträglichkeit von Novesine® 0,4% Augentropfen im Vergleich zur Augentropfengrundlage bei zur Tono... | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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