- Trials with a EudraCT protocol (373)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
373 result(s) found for: Functional groups.
Displaying page 1 of 19.
EudraCT Number: 2018-004875-11 | Sponsor Protocol Number: CAMG334AIT03 | Start Date*: 2019-05-29 | |||||||||||
Sponsor Name:NOVARTIS FARMA S.P.A. | |||||||||||||
Full Title: A RandomizEd, double-blind, cross-over Study to assess Erenumab effecT on BRAIN networks function and structure in comparison to placebo in episodic migraine patients (RESET BRAIN) | |||||||||||||
Medical condition: Episodic migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004287-56 | Sponsor Protocol Number: CHUBX2016/44 | Start Date*: 2019-11-21 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Randomized placebo-controlled trial comparing Methotrexate vs. Methotrexate/Metformin association in rheumatoid arthritis patients: METorMET² study | |||||||||||||
Medical condition: rheumatoid arthritis (RA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005062-30 | Sponsor Protocol Number: NF001 | Start Date*: 2015-06-02 |
Sponsor Name:University Hospital Germans Trias i Pujol | ||
Full Title: Randomized, double-blind, placebo controlled clinical trial to assess the phrenic nerve functional status after periphrenic lidocaine infiltration in lung resection surgery. | ||
Medical condition: Ipsilateral shoulder pain after thoracotomy for lung resection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004202-25 | Sponsor Protocol Number: PI18/01297 | Start Date*: 2019-06-05 | |||||||||||
Sponsor Name:Luis Nombela Franco | |||||||||||||
Full Title: Usefulness of amiodarone for the Prevention of new onset Atrial Fibrillation after transcatheter aortic valve implantation: a randomized controlled trial | |||||||||||||
Medical condition: atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000846-32 | Sponsor Protocol Number: SELEIS | Start Date*: 2014-11-06 | |||||||||||
Sponsor Name:Fundació Privada Hospital Asil de Granollers | |||||||||||||
Full Title: EFFECT OF SEROTONIN AND LEVODOPA FUNCTIONAL RECOVERY IN PATIENTS WITH CEREBRAL INFARCTION | |||||||||||||
Medical condition: Functional recovery in patients with cerebral infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001252-41 | Sponsor Protocol Number: NA | Start Date*: 2022-07-08 |
Sponsor Name:CHU de Liège | ||
Full Title: Preventing postoperative anaemia in total knee arthroplasty and impact of intravenous iron supplementation on postoperative functional recovery : a randomized clinical trial | ||
Medical condition: Total Knee Arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000913-30 | Sponsor Protocol Number: Nath1/2008 | Start Date*: 2008-10-13 | |||||||||||
Sponsor Name:NATHURA SRL | |||||||||||||
Full Title: A symbiotic for the treatment of functional constipation | |||||||||||||
Medical condition: Functional crhonic constipation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003863-67 | Sponsor Protocol Number: FME_2018_9 | Start Date*: Information not available in EudraCT |
Sponsor Name:Fondation Ophtalmologique Adolphe de Rothschild | ||
Full Title: Multicenter randomized controlled trial on the interest of intravitreal injections of anti-VEGF as initial and adjuvant treatment in Coats disease | ||
Medical condition: Coats disease | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003521-34 | Sponsor Protocol Number: CHUBX2015/14 | Start Date*: 2015-10-09 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: Hypertrophic CARdiomyopathy symptom release by alpha stimulant MIDOdrine | ||
Medical condition: Hypertrophic cardiomyopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003282-16 | Sponsor Protocol Number: HA006 | Start Date*: 2005-11-04 |
Sponsor Name:Nuvelo, Inc. | ||
Full Title: PHASE 3, MULTICENTER, MULTI-NATIONAL, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ALFIMEPRASE IN SUBJECTS WITH OCCLUDED CENTRAL VENOUS ACCESS DEVICES | ||
Medical condition: Central venous access device occlusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002688-14 | Sponsor Protocol Number: 201510 | Start Date*: 2015-02-11 | |||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||||||||||||
Full Title: A Phase II, randomised, observer-blind, controlled, multi-country study to assess the safety, reactogenicity and immunogenicity of a single intramuscular dose of different formulations of GlaxoSmit... | |||||||||||||||||||||||
Medical condition: Healthy, non-pregnant women (intended indication: prevention of severe RSV disease in infants by transfer of maternal antibodies following active single dose immunisation of pregnant women) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-004133-16 | Sponsor Protocol Number: IH141 | Start Date*: 2015-02-19 |
Sponsor Name:Hull and east Yorkshire Hospitals Trust | ||
Full Title: Exploratory multicentre prospective double blinded randomised controlled pilot study of the effect of intravenous iron supplementation(Monofer)in iron deficient but not anaemic patients with Chroni... | ||
Medical condition: Chronic Kidney Disease stages 3b to 5 with iron deficiency | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002636-16 | Sponsor Protocol Number: VUMC-ANW-MS-GG-062017 | Start Date*: 2017-10-09 |
Sponsor Name:VU University medical center Amsterdam | ||
Full Title: Cognitive impairment and functional reorganization in multiple sclerosis: The role of GABA and glutamate | ||
Medical condition: Multiple Sclerosis (MS). And specifically cognitive problems in MS. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001387-39 | Sponsor Protocol Number: 1.4 | Start Date*: 2019-03-15 |
Sponsor Name:Thoraxklinik-Heidelberg gGmbH | ||
Full Title: A prospective, randomized, controlled trial to assess the effect of long-term oxygen therapy on 6-minute walking distance, clinical parameters and hemodynamics in patients with pulmonary arterial h... | ||
Medical condition: pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003260-20 | Sponsor Protocol Number: 20140727 | Start Date*: 2016-05-04 |
Sponsor Name:Leiden University Medical Centre | ||
Full Title: CHAMP: Children with Arthritis: Monotherapy or Polytherapy. A multicentre, single-blinded, randomized treat to target, one-year follow-up clinical trial in patients with recent onset Juvenile Idiop... | ||
Medical condition: Juvenile idiopathic arthritis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021722-35 | Sponsor Protocol Number: HYKP1015 | Start Date*: 2010-10-08 | |||||||||||
Sponsor Name:Moorfields Eye Hospital | |||||||||||||
Full Title: Diabetic macula oedema: A prospective randomised study comparing the detailed functional and anatomical changes of repeated pan anti-VEGF therapy with ranibizumab versus conventional macular laser ... | |||||||||||||
Medical condition: Diabetic macular oedema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000848-24 | Sponsor Protocol Number: SB-223412/068 | Start Date*: 2004-10-26 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: An Eight-Week, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate Efficacy and Safety of Talnetant in Subjects with Irritable Bowel Syndrome | |||||||||||||
Medical condition: Irritable Bowel Syndrome (IBS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Prematurely Ended) ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001986-34 | Sponsor Protocol Number: T151/2019 | Start Date*: 2019-11-19 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Exploring the impact of pertussis immunization during pregnancy on the differences in immune response of infants after primary immunization with an acellular pertussis containing vaccine: an open l... | |||||||||||||
Medical condition: Pertussis Infection | |||||||||||||
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Population Age: In utero, Newborns, Infants and toddlers, Children, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002440-14 | Sponsor Protocol Number: AC-055-302 | Start Date*: 2008-05-15 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd. | |||||||||||||
Full Title: A multicenter, double-blind, randomized, placebo-controlled, parallel group, event-driven, Phase III study to assess the effects of ACT-064992 on morbidity and mortality in patients with symptomati... | |||||||||||||
Medical condition: To assess the effects of ACT-064992 on morbidity and mortality in patients with symptomatic pulmonary arterial hypertension | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) DE (Completed) NL (Completed) FR (Completed) FI (Completed) SE (Completed) AT (Completed) DK (Completed) SK (Completed) PT (Prematurely Ended) IT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011853-42 | Sponsor Protocol Number: NALCOL 01 | Start Date*: 2009-12-22 | |||||||||||
Sponsor Name:Norfolk and Norwich University Hospital NHS Trust | |||||||||||||
Full Title: NALOXONE HYDROCHLORIDE SR GASTRO-RESISTANT SUSTAINED RELEASE CAPSULES AS A TREATMENT FOR FUNCTIONAL CONSTIPATION: A RANDOMISED, DOUBLE BLIND CONTROLLED TRIAL IN SECONDARY CARE | |||||||||||||
Medical condition: Functional constipation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
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