- Trials with a EudraCT protocol (10,988)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
10,988 result(s) found.
Displaying page 108 of 550.
EudraCT Number: 2013-002966-38 | Sponsor Protocol Number: CCD-01535BC1-02 | Start Date*: 2013-11-20 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A PHASE II, PARTIAL-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, 5-WAY CROSS-OVER CLINICAL PHARMACOLOGY STUDY TO EVALUATE THE PHARMACODYNAMICS OF BDP/B17MP AND FORMOTEROL ACROSS TWO DIFFERENT DOSE LEVELS... | |||||||||||||
Medical condition: COPD patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005570-56 | Sponsor Protocol Number: GLINT | Start Date*: 2014-01-28 |
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | ||
Full Title: Glucose Lowering In Non-diabetic hyperglycaemia Trial (GLINT) - a randomised controlled trial to establish the effectiveness and cost-effectiveness of metformin in preventing cardiovascular events ... | ||
Medical condition: Non-diabetic hyperglycaemia (elevated blood glucose levels below the diagnostic threshold for diabetes) and high risk of cardiovascular disease (>20% risk over 10 years) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-005565-20 | Sponsor Protocol Number: QMUL111111 | Start Date*: 2012-05-02 | |||||||||||
Sponsor Name:QUEEN MARY, UNIVERSITY OF LONDON | |||||||||||||
Full Title: Comparison of the effects of the electronic cigarette and nicotine inhalator on tobacco withdrawal symptoms over 24 hours of abstinence | |||||||||||||
Medical condition: Nicotine withdrawal state | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005581-37 | Sponsor Protocol Number: 5946 | Start Date*: 2012-08-06 | |||||||||||
Sponsor Name:The Newcastle upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Efficacy of Switch to Lopinavir/Ritonavir in Improving Cognitive function in Efavirenz treated patients | |||||||||||||
Medical condition: Cognitive function and sleep pattern in HIV-1 patients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001784-13 | Sponsor Protocol Number: ISRCTN91422391 | Start Date*: 2014-12-29 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: PROVENT: A randomised, double blind, placebo controlled feasibility study to examine the clinical effectiveness of aspirin and/or Vitamin D3 to prevent disease progression in men on active surveill... | |||||||||||||
Medical condition: Prostate cancer disease progression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000292-15 | Sponsor Protocol Number: S241-GB-10 | Start Date*: 2006-03-13 | |||||||||||
Sponsor Name:Stiefel Laboratories Maidenhead Ltd. | |||||||||||||
Full Title: A Phase II, Single-Centre, Randomised,Double-Blind, Parallel Group, CPO Solution, Dose Range Finding Study in Subjects with Seborrhoeic Dermatitis of the Scalp | |||||||||||||
Medical condition: Seborrhoeic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002068-25 | Sponsor Protocol Number: CSLCT-NHF-05-13 | Start Date*: 2006-05-23 |
Sponsor Name:CSL Limited | ||
Full Title: A Single Site, Open-Label Study to Evaluate the Immunogenicity and Safety of Enzira in Healthy 'Adults' aged >18 to <60 years and in Healthy 'Older Adults' aged >60 years for the 2006/2007 Northern... | ||
Medical condition: Prophylaxis of influenza | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004902-16 | Sponsor Protocol Number: | Start Date*: 2007-10-01 | |||||||||||||||||||||
Sponsor Name:Royal Bournemouth Hospital | |||||||||||||||||||||||
Full Title: A randomized phase II trial to determine whether the application of imiquimod cream to the vaccination site can improve the immune responsiveness to influenza vaccination in patients with untreated... | |||||||||||||||||||||||
Medical condition: Early stage (Binet stage A) Patients with chronic lymphocytic leukaemia and control group of age and sex matched healthy volunteers | |||||||||||||||||||||||
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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: 2007-003291-19 | Sponsor Protocol Number: VAI01 | Start Date*: 2009-07-30 | ||||||||||||||||
Sponsor Name:University of Dundee | ||||||||||||||||||
Full Title: A proof of concept study to evaluate if concomitant topical intranasal steroid prevents tolerance and rebound congestion due to regular oxymetazoline in persistent allergic rhinitis | ||||||||||||||||||
Medical condition: Allergic Rhinitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001811-40 | Sponsor Protocol Number: PAW01 | Start Date*: 2008-08-27 | |||||||||||
Sponsor Name:The University of Dundee | |||||||||||||
Full Title: A Proof of Concept Study to Evaluate the Additive Effects of HFA-BDP (Qvar) to fluticasone/salmeterol (Seretide) on Surrogate Markers of Small and Large Airway Inflammation in Refractory Asthma | |||||||||||||
Medical condition: Severe refractory asthma. | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005566-39 | Sponsor Protocol Number: 06_DOG07_64 | Start Date*: 2008-03-05 | ||||||||||||||||
Sponsor Name:Christie Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: Concurrent chemoradiotherapy for stage III non small cell lung cancer followed by consolidation pemetrexed: a phase II study | ||||||||||||||||||
Medical condition: Non-small cell lung cancer, stage III | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000517-30 | Sponsor Protocol Number: 3065 | Start Date*: 2009-03-26 | |||||||||||
Sponsor Name:The Royal Marsden Hospital NHS Trust | |||||||||||||
Full Title: A multicentre randomised phase II clinical study of UFT/leucovorin (LV), radiotherapy with or without cetuximab following induction gemcitabine plus capecitabine in patients with locally advanced p... | |||||||||||||
Medical condition: Locally-advanced (unresectable) pancreatic adenocarcinoma, undifferentiated carcinoma or non-small cell carcinoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001723-19 | Sponsor Protocol Number: EC001(MenC1) | Start Date*: 2006-06-02 |
Sponsor Name:University of Bristol | ||
Full Title: AN OPEN LABEL, SINGLE CENTRE PILOT STUDY TO EVALUATE THE KINETICS OF THE SYSTEMIC B-CELL IMMUNE RESPONSE TO A MENINGOCOCCAL SEROGROUP C CONJUGATE VACCINE IN HEALTHY ADULTS | ||
Medical condition: Meningococcal serogroup C infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-008141-37 | Sponsor Protocol Number: diab123v1.0 | Start Date*: 2009-09-08 | ||||||||||||||||
Sponsor Name:Sherwood Forest Hospitals Foundation Trust | ||||||||||||||||||
Full Title: Effects of Exenatide on excess daytime sleepiness (EDS), wakefulness and driving performance in obese type-2 diabetes patients without sleep apnea – proof of concept study | ||||||||||||||||||
Medical condition: sleepiness and lethargy among obese patients with diabetes | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002137-37 | Sponsor Protocol Number: T-004 | Start Date*: 2007-07-13 | |||||||||||
Sponsor Name:TRIO Medicines Ltd | |||||||||||||
Full Title: Does adding YF476 to amoxicillin and clarithromycin aid eradication of H. pylori from healthy carriers? | |||||||||||||
Medical condition: H pylori carriage in healthy adults | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003285-42 | Sponsor Protocol Number: PHT/2005/37 | Start Date*: 2005-11-28 |
Sponsor Name:Portsmouth Institution Medicine, Health & Social Care, Portsmouth University [...] | ||
Full Title: A RCT to test the analgesic efficacy of topical morphine on minor and partial thickness burns in A&E | ||
Medical condition: Minor superficial and partial thickness burns <5% body surface area. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003596-12 | Sponsor Protocol Number: C/21/07 | Start Date*: 2008-01-28 | |||||||||||
Sponsor Name:Imperial College of Science Technology and Medicine | |||||||||||||
Full Title: A neoadjuvant study of chemotherapy versus endocrine therapy in postmenopausal patients with primary breast cancer | |||||||||||||
Medical condition: This trial will involve postmenopausal patients with histologically confirmed breast tumours in whom it is felt cytoreductive systemic therapy would enable conservative surgery to be carried out. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2007-000774-23 | Sponsor Protocol Number: CCD-0701-PR-0020 | Start Date*: 2007-05-10 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A | |||||||||||||
Full Title: EVALUATION OF CARDIAC SAFETY, TOLERABILITY AND EFFICACY OF CUMULATIVE DOSES OF CHF5188 pMDI (FIXED COMBINATION BUDESONIDE/CARMOTEROL 200/1 µg) COMPARED TO SAME CUMULATIVE DOSES OF CARMOTEROL pMDI A... | |||||||||||||
Medical condition: Stable persistent asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000056-14 | Sponsor Protocol Number: 06/DTD/3791E | Start Date*: 2008-03-03 | ||||||||||||||||
Sponsor Name:Cardiff University | ||||||||||||||||||
Full Title: Determination of method-specific normal cortisol and adrenal hormone responses to the short Synacthen test | ||||||||||||||||||
Medical condition: Normal, healthy volunteers to establish a reference range for the synacthen test, plus patients with hypoadrenalism/hypopituitarism | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-006362-41 | Sponsor Protocol Number: RM06/8013 | Start Date*: 2007-04-05 | |||||||||||
Sponsor Name:Leeds Teaching Hospital NHS Trust | |||||||||||||
Full Title: An open study on the pharmacokinetics and safety of oral voriconazole in adult patients with cystic fibrosis | |||||||||||||
Medical condition: Adult patients with cystic fibrosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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