- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
15 result(s) found for: Health literacy.
Displaying page 1 of 1.
EudraCT Number: 2006-005444-88 | Sponsor Protocol Number: TH9507-CTR-1011 | Start Date*: 2007-01-16 | |||||||||||
Sponsor Name:Theratechnologies Inc. | |||||||||||||
Full Title: A Multicenter, Double-blind, Randomized, Placebo-Controlled Study Assessing the Efficacy and Safety of a 2 mg dose of TH9507, a Growth Hormone-Releasing Factor Analog, in HIV Subjects with Excess A... | |||||||||||||
Medical condition: HIV-associated lipodystrophy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) GB (Completed) DE (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000235-51 | Sponsor Protocol Number: ANZUP1301 | Start Date*: 2020-11-11 |
Sponsor Name:Nottingham University Hospitals NHS Trust | ||
Full Title: BCG+MM Trial Adding mitomycin to BCG as adjuvant intravesical therapy for high-risk, non–muscle-invasive bladder cancer: a randomised phase 3 trial | ||
Medical condition: High grade non muscle invasive bladder cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000397-31 | Sponsor Protocol Number: 6106A1-500 | Start Date*: 2005-05-09 |
Sponsor Name:Wyeth Vaccines Research | ||
Full Title: A Randomized Controlled Open-Label Phase IV Multi Center Study to Assess the Effect of Antipyretic Prophylactic Treatment on the Rate of Febrile Reactions Following Concomitant Contralateral Admini... | ||
Medical condition: Healthy infants who shall receive their first routine vaccination. | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014424-29 | Sponsor Protocol Number: H6L-MC-LFBF (b) | Start Date*: 2010-02-05 |
Sponsor Name:Eli Lilly and Company | ||
Full Title: Open-Label Extension for Alzheimer’s Disease Patients Who Complete One of Two Semagacestat Phase 3 Double-Blind Studies (H6L-MC-LFAN or H6L-MC-LFBC) | ||
Medical condition: Alzheimer's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) DE (Completed) ES (Prematurely Ended) BE (Completed) IT (Completed) FR (Completed) SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000344-21 | Sponsor Protocol Number: MP1032-CT05 | Start Date*: 2021-07-21 | ||||||||||||||||||||||||||
Sponsor Name:MetrioPharm AG | ||||||||||||||||||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER, PROOF-OF-CONCEPT, PHASE IIA STUDY OF MP1032 PLUS STANDARD OF CARE VS STANDARD OF CARE IN THE TREATMENT OF HOSPITALIZED PATIENTS WITH MOD... | ||||||||||||||||||||||||||||
Medical condition: Moderate to severe coronavirus disease 2019 (COVID 19) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) HU (Completed) ES (Ongoing) BG (Completed) IT (Completed) RO (Ongoing) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001397-30 | Sponsor Protocol Number: APOS | Start Date*: 2021-03-17 | |||||||||||
Sponsor Name:Ruprecht-Karls-University Heidelberg, Medical Faculty rep. by University hospital and Commercial Managing Director | |||||||||||||
Full Title: APOS study- Antibiotic Prophylaxis for preventing infectious complications in Orthognathic Surgery | |||||||||||||
Medical condition: Prophylaxis of postoperative surgical site infections | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004818-34 | Sponsor Protocol Number: CTRIAL-IE-19-32 | Start Date*: 2021-04-23 | |||||||||||
Sponsor Name:Cancer Trials Ireland | |||||||||||||
Full Title: DASL-HiCaP: Darolutamide Augments Standard Therapy for Localised Very High-Risk Cancer of the Prostate (ANZUP1801). A randomised phase 3 double-blind, placebo-controlled trial of adding darolutamid... | |||||||||||||
Medical condition: Clinically localised prostate cancer defined as very high risk, or with very high risk features. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003191-23 | Sponsor Protocol Number: ANZUP1303 | Start Date*: 2014-11-07 | |||||||||||
Sponsor Name:Cancer Trials Ireland | |||||||||||||
Full Title: Randomised phase 3 trial of enzalutamide in androgen deprivation therapy with radiation therapy for high risk, clinically localised, prostate cancer: ENZARAD | |||||||||||||
Medical condition: Localised prostate cancer at high risk of recurrence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IE (Trial now transitioned) GB (GB - no longer in EU/EEA) BE (Completed) AT (Trial now transitioned) ES (Ongoing) SI (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000116-30 | Sponsor Protocol Number: 63733657ALZ2002 | Start Date*: 2021-04-07 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Assess the Efficacy and Safety of JNJ-63733657, an Anti-tau Monoclonal Antibody, in Participants with Early Alzh... | |||||||||||||
Medical condition: Early Alzheimer’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003337-15 | Sponsor Protocol Number: CLR_18_06 | Start Date*: 2019-06-18 | |||||||||||
Sponsor Name:Sun Pharma Advanced Research Company (SPARC) Limited | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study of K0706 in Subjects With Early Parkinson’s Disease | |||||||||||||
Medical condition: Early Parkinson’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) SK (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003190-42 | Sponsor Protocol Number: ANZUP1304 | Start Date*: 2014-10-17 | ||||||||||||||||
Sponsor Name:Cancer Trials Ireland | ||||||||||||||||||
Full Title: Randomised phase 3 trial of enzalutamide in first line androgen deprivation therapy for metastatic prostate cancer: ENZAMET | ||||||||||||||||||
Medical condition: Metastatic Prostate Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IE (Trial now transitioned) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021155-11 | Sponsor Protocol Number: H8A-MC-LZAO | Start Date*: 2010-11-29 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Continued Efficacy and Safety Monitoring of Solanezumab, an Anti-Amyloid β Antibody in Patients with Alzheimer’s Disease | |||||||||||||
Medical condition: Alzheimer's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Completed) IT (Completed) SE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004977-42 | Sponsor Protocol Number: CB-01-11/28 | Start Date*: 2017-11-10 | |||||||||||
Sponsor Name:Cosmo Technologies Ltd. | |||||||||||||
Full Title: A Phase II, multicentre, randomised, double-blind, placebo controlled, proof of concept study of efficacy and safety of Rifamycin SV-MMX® 600 mg tablets administered three or two times daily to pat... | |||||||||||||
Medical condition: Diarrhoea-predominant irritable bowel syndrome (IBS-D) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Temporarily Halted) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004243-39 | Sponsor Protocol Number: VHCRP1401 | Start Date*: 2016-11-17 | |||||||||||
Sponsor Name:University of New South Wales Australia | |||||||||||||
Full Title: A randomised study of interferon-free treatment for recently acquired hepatitis C in people who inject drugs and people with HIV coinfection. | |||||||||||||
Medical condition: Recent hepatitis C virus infection all genotypes. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001165-27 | Sponsor Protocol Number: 191-078 | Start Date*: 2014-11-06 | |||||||||||
Sponsor Name:Mylan Pharma UK Ltd | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel Group 24 Week Placebo-Controlled Efficacy and Safety Study with a 28 Week Long Term Extension, of Nebulized Fluticasone Propionate (FP) /Formoterol Fumarate (FF... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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