- Trials with a EudraCT protocol (139)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
139 result(s) found for: False Consensus Effect.
Displaying page 1 of 7.
EudraCT Number: 2006-003194-27 | Sponsor Protocol Number: ML3602 | Start Date*: 2006-08-02 | |||||||||||
Sponsor Name:University Hospitals KU Leuven | |||||||||||||
Full Title: mirtazapine versus placebo in functional dyspepsia: a randomized, double-blind, placebo-controlled trial | |||||||||||||
Medical condition: functional dyspepsia diagnosed according to international consensus criteria ("Rome II criteria") | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023828-24 | Sponsor Protocol Number: 09107 | Start Date*: 2011-06-09 |
Sponsor Name:University of Nottingham | ||
Full Title: The effect of Thalidomide on sputum biomarkers in IPF cough. | ||
Medical condition: Cough in Idiopathic Pulmonary fibrosis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-001425-26 | Sponsor Protocol Number: REDOX19032019 | Start Date*: 2019-07-04 |
Sponsor Name:Thoraxcentrum Erasmus MC | ||
Full Title: Rotterdam Edoxaban Leaflet Evaluation in Patients after Transcatheter Aortic Valve Implantation | ||
Medical condition: aortic stenosis | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002116-10 | Sponsor Protocol Number: i3.1_IBS+SIBO | Start Date*: 2019-09-27 |
Sponsor Name:AB-Biotics S.A. | ||
Full Title: Interventional post-marketing study to evaluate i3.1 efficacy on SIBO (Small Intestinal Bacterial Overgrowth)reduction in IBS (Irritable bowel syndrom) patients | ||
Medical condition: Irritable Bowel Syndrome (IBS) + Small Intestinal Bacterial Overgrowth (SIBO) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001002-83 | Sponsor Protocol Number: IDT.ES.LEV.12006 | Start Date*: 2006-06-06 |
Sponsor Name:Hospital Clinico San Carlos, Unidad de Investigacion Cardiovascular | ||
Full Title: Pilot study to evaluate the effect of vardenafil treatment on the proteomic pattern of mononuclear cells and serum proteins in patients with erectile dysfunction and mellitus diabetes. | ||
Medical condition: Erectile Dysfuntion | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004357-82 | Sponsor Protocol Number: OSU6162ME1 | Start Date*: 2012-02-21 |
Sponsor Name:A. Carlsson Research AB | ||
Full Title: A randomized controlled trial of OSU6162 in treatment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome | ||
Medical condition: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001529-88 | Sponsor Protocol Number: LOC 04/2004-01 | Start Date*: 2004-11-08 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Dose efficacy relation of inhalative prostaglandin I2 vs. inhalative prostaglandin E1 in patients with ARDS: comparison of efficacy with respect to paO2/FiO2 ratio, Qs/Qt and PAP. | ||
Medical condition: Patients suffering from ARDS who need in the moment of enrolment artificial respiration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-017665-31 | Sponsor Protocol Number: CSE | Start Date*: 2010-09-30 |
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | ||
Full Title: Effect on mother and fetus of epidural and combined spinal-epidural techniques for labour analgesia | ||
Medical condition: Labour | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018586-39 | Sponsor Protocol Number: 2010/0121 | Start Date*: 2010-06-01 |
Sponsor Name:Medical Department M (Endocrinology & Diabetes) | ||
Full Title: Diurnal variation of exogenous peptides | ||
Medical condition: Adults with growth hormone disease (AGHD). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000580-24 | Sponsor Protocol Number: | Start Date*: 2019-05-17 |
Sponsor Name:Hull & East Yorkshire Hospitals NHS trust | ||
Full Title: A single arm, open-label clinical trial of azithromycin in pulmonary sarcoidosis | ||
Medical condition: Sarcoidosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-004929-33 | Sponsor Protocol Number: SiccaIkervis | Start Date*: 2018-12-05 |
Sponsor Name:KH Hietzing, Department of Ophthalmology | ||
Full Title: Effect of Ciclosporin eyedrops on ocular symptoms and optical image quality in patients with primary or secondary Sjögren syndrome | ||
Medical condition: primary or secondary Sjögren Syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000820-34 | Sponsor Protocol Number: P03548 | Start Date*: 2006-08-31 |
Sponsor Name:Integrated Therapeutics Group, Incorporated-a subsidiary of Schering Plough | ||
Full Title: Comparison of Three Regimens of PEG-Intron plus Ribavirin in the Treatment of Chronic Hepatitis C, Genotype 2 or 3, in Previously Untreated Patients | ||
Medical condition: Chronic Hepatitis C, Genotype 2 or 3 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PT (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015729-35 | Sponsor Protocol Number: PCOS&Niacin | Start Date*: 2009-11-23 |
Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | ||
Full Title: TO DETERMINE IF CARDIOVASCULAR RISK INDICES INCLUDING POSTPRANDIAL HYPERTRIGLYCERIDAEMIA ARE MODIFIED FAVOURABLY BY NICOTINIC ACID (NIACIN) IN PATIENTS WITH POLYCYSTIC OVARY SYNDROME (PCOS) | ||
Medical condition: Polycystic ovary syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000702-29 | Sponsor Protocol Number: LORALAM-2020 | Start Date*: 2021-06-07 | |||||||||||
Sponsor Name:IDIBELL (Institut d’Investigació Biomédica de Bellvitge) | |||||||||||||
Full Title: Phase-II randomized clinical trial to evaluate the effect of Loratadine associated with Rapamune on Lymphagioleiomyomatosis (LAM). | |||||||||||||
Medical condition: EFFECT OF LORATADINE ON LYMPHANGIOLEIOMYOMATOSIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017245-64 | Sponsor Protocol Number: OG09/9146 | Start Date*: 2010-09-07 |
Sponsor Name:Leeds Teaching Hospitals NHS Trust | ||
Full Title: The effect of metformin co-treatment in hormone-replacement frozen embryo replacement cycles in women with polycystic ovary syndrome. | ||
Medical condition: Polycystic Ovary Syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-001414-33 | Sponsor Protocol Number: RGHT 000275 | Start Date*: 2006-08-01 |
Sponsor Name:The Royal Group Hospitals Trust | ||
Full Title: The effect of hydroxyl-methyl coenzyme A reductase inhibition (statins) in patients with acute lung injury(ALI) and the acute respiratory distress syndrome(ARDS) | ||
Medical condition: Acute Lung Injury (ALI) and the Acute Respiratory Distress Syndrome (ARDS) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-003761-33 | Sponsor Protocol Number: IDT.ES.LEV.12004-EMDE | Start Date*: 2005-02-17 |
Sponsor Name:Unidad de Neuroinmunología | ||
Full Title: Unicenter double-blind, cross-over, randomised, placebo controlled clinical trial to evaluate efficacy of vardenafil in subjects with E.D. and multiple sclerosis (M.S.) | ||
Medical condition: Erectile Dysfunction | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000677-77 | Sponsor Protocol Number: S61338 | Start Date*: 2018-06-26 |
Sponsor Name:University Hospital Leuven | ||
Full Title: Novel strategies in weight loss in women with polycystic ovary syndrome: does the gut microbiome play a role? | ||
Medical condition: overweight and obese women with polycystic ovary syndrome (PCOS) at risk for metabolic syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023529-39 | Sponsor Protocol Number: RHM CHI 0548 | Start Date*: 2011-02-18 |
Sponsor Name:Southampton University Hopsitals NHS Trust | ||
Full Title: Reducing antibiotic tolerance using low dose nitric oxide in cystic fibrosis – a phase 2 pilot study | ||
Medical condition: Cystic Fibrosis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-003766-27 | Sponsor Protocol Number: 848015011 | Start Date*: 2018-07-18 | |||||||||||
Sponsor Name:VU University Medical Centre | |||||||||||||
Full Title: The DREAMING study: Efficacy of low dose amitriptyline and mirtazapine for insomnia disorder: a double-blind, randomized, placebo-controlled trial in general practice | |||||||||||||
Medical condition: Insonnia disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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