- Trials with a EudraCT protocol (1,315)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
1,315 result(s) found for: Lifestyle.
Displaying page 8 of 66.
EudraCT Number: 2012-004900-37 | Sponsor Protocol Number: DC05/RUP/I/13 | Start Date*: 2012-11-20 |
Sponsor Name:J. Uriach y Compañía, S.A. | ||
Full Title: A Phase I, Randomised, Double-blind, Placebo-controlled, Parallel group study to assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of oral Rupatadine in Healthy Japanese Subjec... | ||
Medical condition: This is a Phase I study in helathy subjects. No condition is being treated. The IMP is approved for symptomatic treatment of allergic rhinitis and urticaria in adults and adolescents (over 12 yea... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-007026-22 | Sponsor Protocol Number: CL2-09490-157 | Start Date*: 2008-03-28 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Assessment of the effects on 24-hour ambulatory blood pressure and the safety of a once-a-day oral 8 mg perindopril morning administration versus evening administration in hypertensive patients. An... | |||||||||||||
Medical condition: Essential arterial hyperpertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024283-18 | Sponsor Protocol Number: AF219-006 | Start Date*: 2011-05-20 | |||||||||||
Sponsor Name:Afferent Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Study to Assess the Efficacy of AF-219, a P2X3 Receptor Antagonist, in Subjects with Chronic Cough | |||||||||||||
Medical condition: Subjects with Chronic Cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000332-25 | Sponsor Protocol Number: version1 | Start Date*: 2012-06-19 |
Sponsor Name:University of Birmingham | ||
Full Title: vitamin D replacement to prevent lung injury following oesophagectomy - a randomised controlled trial. | ||
Medical condition: perioperative inflammation in patients undergoing oesophagectomy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001587-70 | Sponsor Protocol Number: 07/03 Inopec ITEM | Start Date*: 2007-06-07 |
Sponsor Name:Fraunhofer Gesellschaft | ||
Full Title: A randomized, double-blind, placebo-controlled crossover study to assess the efficacy's reproducibility of a combination of Pseudoephedrine and Cetirizine on symptom scores and rhinomanometry in pa... | ||
Medical condition: subjects with seasonal allergic rhinitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001594-40 | Sponsor Protocol Number: UNOLE0526 | Start Date*: 2016-05-10 | |||||||||||
Sponsor Name:University of Leicester | |||||||||||||
Full Title: SGLT-2 Inhibitor Empagliflozin Effects on Appetite and Weight Regulation: A randomised double-blind placebo-controlled trial (SEESAW) | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005196-16 | Sponsor Protocol Number: H8O-MC-GWBQ | Start Date*: 2012-07-24 | |||||||||||
Sponsor Name:Amylin Pharmaceuticals, Inc. | |||||||||||||
Full Title: Safety and Efficacy of Exenatide as Monotherapy and Adjunctive Therapy to Oral Antidiabetic Agents in Adolescents with Type 2 Diabetes | |||||||||||||
Medical condition: Treatment of Type 2 diabetes mellitus | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006844-21 | Sponsor Protocol Number: DELP-01 | Start Date*: 2009-12-01 | |||||||||||
Sponsor Name:Dermal Laboratories Ltd | |||||||||||||
Full Title: Evaluation of a developmental ‘long lasting’ emollient in subjects with dry skin. | |||||||||||||
Medical condition: Eczema sufferers with dry skin. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001715-36 | Sponsor Protocol Number: RD.03.SPR.115828 | Start Date*: 2017-10-23 | |||||||||||
Sponsor Name:GALDERMA R&D, SNC | |||||||||||||
Full Title: A study to assess the safety and efficacy of nemolizumab (CD14152) in subjects with prurigo nodularis (PN) | |||||||||||||
Medical condition: Prurigo nodularis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) FR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004435-20 | Sponsor Protocol Number: | Start Date*: 2017-06-08 |
Sponsor Name:Research & Development Department, Hull & East Yorkshire Hospitals NHS Trust | ||
Full Title: The effect of empagliflozin versus metformin on hormonal, metabolic and cardiovascular risk factors in patients with polycystic ovary syndrome (PCOS) – a randomised open-label parallel study. | ||
Medical condition: Polycystic ovary syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001731-28 | Sponsor Protocol Number: C LF 23-0121 0401 | Start Date*: 2004-09-24 |
Sponsor Name:FOURNIER Laboratories Ireland | ||
Full Title: A double-blind, 3-arm study on weight loss with combination of micronised fenofibrate 267 mg and metformin 1700 mg per day compared to metformin 1700 mg and placebo, at 6 months, in obese patients,... | ||
Medical condition: Obesity | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002266-40 | Sponsor Protocol Number: CAIN457ADE02 | Start Date*: 2013-12-09 |
Sponsor Name:Novartis Pharma GmbH | ||
Full Title: A randomized, double-blind, placebo-controlled, multicenter, exploratory evaluation of surrogate markers of cardiovascular risk in patients with active chronic plaque-type psoriasis treated for 52 ... | ||
Medical condition: active chronic plaque-type psoriasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000106-41 | Sponsor Protocol Number: CXA100750 | Start Date*: 2004-09-07 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A study to investigate the effect of GW406381 on methotrexate pharmacokinetics in patients treated with methotrexate for rheumatoid arthritis | ||
Medical condition: The patients entering the trial have rheumatoid arthritis although treatment of the disease itself is not under investigation in this study. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004526-72 | Sponsor Protocol Number: 1 | Start Date*: 2006-03-02 |
Sponsor Name:Addenbrooke's NHS Trust | ||
Full Title: A randomised controlled study of continuous subcutaneous insulin infusion (CSII) therapy compared to conventional bolus insulin treatment in preschool aged children with Type 1 diabetes. | ||
Medical condition: Type 1 Diabetes Mellitus | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-002976-14 | Sponsor Protocol Number: CRI103143 | Start Date*: 2006-09-27 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: A phase IIa, single-centre, randomised, placebo-controlled, double-blind, three-period crossover exploratory study investigating the effects on gut autonomic responses of single administrations of ... | ||
Medical condition: Irritable Bowel Syndrome (IBS) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003544-27 | Sponsor Protocol Number: PRV-06009 | Start Date*: 2006-07-21 | |||||||||||
Sponsor Name:Provident Clinical Research & Consulting, Inc. | |||||||||||||
Full Title: An Evaluation of Simvastatin 20 mg Plus Omacor 4 g Compared to Simvastatin 20 mg Plus Placebo in Subjects with Mixed Dyslipidemia | |||||||||||||
Medical condition: mixed dyslipidemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000443-99 | Sponsor Protocol Number: MIGAN | Start Date*: 2008-04-09 | |||||||||||
Sponsor Name:Universitätsklinikum Ulm | |||||||||||||
Full Title: Comparison of the sequential maintenance therapy with Mycophenolat and Prednisolon to standard therapy after completed induction therapy – a multicenter, randomised, phase III intervention study fo... | |||||||||||||
Medical condition: progressive IgA-Nephritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000552-18 | Sponsor Protocol Number: 769 | Start Date*: 2014-01-30 |
Sponsor Name:Bausch & Lomb Incorporated | ||
Full Title: A Randomized, Multicenter, Double-Masked, Parallel-Group Study Comparing the Safety and Efficacy of BOL-303259-X 0.024% (Latanoprostene Bunod) Ophthalmic Solution With Timolol Maleate Ophthalmic ... | ||
Medical condition: Open-Angle Glaucoma or Ocular Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001259-37 | Sponsor Protocol Number: D3741C00012 | Start Date*: 2020-06-26 |
Sponsor Name:AstraZeneca AB | ||
Full Title: An Open-Label, Multi-Centre, Phase I Study to Assess the Pharmacokinetics, Pharmacodynamics and Safety of 2-Week Treatment with Inhaled AZD7594 in Adolescents (12 to 17 years) with Asthma | ||
Medical condition: Asthma | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2009-017139-16 | Sponsor Protocol Number: Bay 86-5037/14853 | Start Date*: 2010-06-10 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Effect of exercise alone or in combination with testosterone replacement on muscle strength and quality of life in older men with low testosterone concentrations: a randomized double-blind, placebo... | |||||||||||||
Medical condition: The objective of this study is to determine whether in older men with symptomatic age-associated testosterone deficiency exercise training in combination with testosterone replacement therapy leads... | |||||||||||||
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Population Age: Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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