- Trials with a EudraCT protocol (3,292)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3,292 result(s) found for: Health data.
Displaying page 1 of 165.
EudraCT Number: 2019-004750-28 | Sponsor Protocol Number: PropoCon-Pilot | Start Date*: 2021-04-30 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Electrocardiographic And Clinical Effects Of Target-Controlled Infusion Of Propofol In Adults With Brugada Syndrome. A Pilot Study. | ||
Medical condition: Target Controlled Infusion of Propofol in patients with Brugada Syndrome. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001328-21 | Sponsor Protocol Number: ABR65448 | Start Date*: 2019-01-08 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Chronotherapy with aspirin for reduction of cardiovascular disease | ||
Medical condition: The medical condioton to be investigated is recurrent cardiovascular disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003244-27 | Sponsor Protocol Number: PANORAMIC-Norway | Start Date*: 2023-04-11 | ||||||||||||||||
Sponsor Name:Helse Bergen HF | ||||||||||||||||||
Full Title: PAxlovid loNg cOvid-19 pRevention triAl with recruitMent In the Community in Norwayy | ||||||||||||||||||
Medical condition: COVID-19 SARS-CoV-2 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NO (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004424-65 | Sponsor Protocol Number: 15085MS-AS | Start Date*: 2016-05-09 |
Sponsor Name:Belfast Health and Social Care Trust | ||
Full Title: Prevention of post-operative complications by using HMG-CoA Reductase Inhibitor in patients undergoing oesophagectomy - A multicentre, randomised, double blind, placebo controlled trial | ||
Medical condition: Post-operative complications - Post-operative Pulmonary complication, Acute Respiratory Distress Syndrome and Myocardial Infarction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2010-019513-24 | Sponsor Protocol Number: 10_022 | Start Date*: 2011-03-03 |
Sponsor Name:London School of Hygiene & Tropical Medicine | ||
Full Title: Antibiotics for exacerbations of chronic obstructive pulmonary disease: a pilot randomised trial within the General Practice Research Database | ||
Medical condition: Diagnosed at a GP visit as suffering from acute exacerbation of COPD a. Medical history of COPD b. Increase in dyspnoea AND increase of (non-purulent) sputum volume | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000083-17 | Sponsor Protocol Number: NVI-245 | Start Date*: 2008-03-19 |
Sponsor Name:Nederlands Vaccin Instituut | ||
Full Title: Nasopharyngeal pneumococcal colonization data in infants at the age of 12, 18 and 24 months | ||
Medical condition: Pneumococcal carriership in children having previously received Prevenar vaccination (7-valent pneumococcal conjugate vaccine) according to the 3+1 vaccination schedule used in the Dutch National I... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2020-002101-25 | Sponsor Protocol Number: FDA02_AIM3 | Start Date*: 2020-09-14 |
Sponsor Name:HEALTH – Institute for Biomedicine and Health Sciences, JOANNEUM RESEARCH Forschungsgesellschaft mbH | ||
Full Title: A SINGLE CENTER, OPEN-LABEL, CLINICAL STUDY TO EVALUATE THE ABILITY OF DERMAL OPEN FLOW MICROPERFUSION (DOFM) FOR BIOEQUIVALENCE TESTING OF TOPICALLY APPLIED DICLOFENAC SODIUM PRODUCTS IN HEALTHY S... | ||
Medical condition: Healthy Volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003041-41 | Sponsor Protocol Number: 012507 | Start Date*: 2018-11-16 | |||||||||||||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||||||||||||
Full Title: A pragmatic pilot randomised controlled trial of Prothrombin Complex Concentrate (PCC) versus Fresh Frozen Plasma (FFP) in adult patients who are undergoing Heart Surgery | |||||||||||||||||||||||
Medical condition: Major bleeding during cardiac surgery not related to vitamin K antagonists | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-005005-12 | Sponsor Protocol Number: D2.D12.Bemfola | Start Date*: 2018-05-28 | ||||||||||||||||
Sponsor Name:UZ Brussel | ||||||||||||||||||
Full Title: Initiation of ovarian stimulation with recombinant-human FSH (Bemfola®) in the late follicular phase, a randomised controlled study. | ||||||||||||||||||
Medical condition: Subfertility Oocyte donation | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001314-25 | Sponsor Protocol Number: KIANANDR140701 | Start Date*: 2015-03-10 |
Sponsor Name:Karolinska Institutet | ||
Full Title: The effect of on demand versus continuous use of proton pump inhibitors on reflux symptoms, quality of life and self-rated health in patients with gastro-oesophageal reflux disease | ||
Medical condition: Gastrooesophageal reflux disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2019-001688-66 | Sponsor Protocol Number: SC.14/18-19 | Start Date*: 2019-09-09 | |||||||||||
Sponsor Name:University of Warwick [...] | |||||||||||||
Full Title: Sugar or Salt (SOS) trial: Hyperosmolar therapy in traumatic brain injury | |||||||||||||
Medical condition: Increased intracranial pressure following traumatic brain injury | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001563-12 | Sponsor Protocol Number: 20142017 | Start Date*: 2015-02-16 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Efficacy of Single inhaler Maintenance And Reliever Therapy (SMART) with Spiromax® budesonide/formoterol versus fixed dose treatment with Diskus® fluticasone/salmeterol in COPD | ||
Medical condition: Chronic obstructive pulmonary disease (COPD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000663-45 | Sponsor Protocol Number: PREVENT-iT-2021.07 | Start Date*: 2023-02-01 |
Sponsor Name:Hamilton Health Sciences Corporation | ||
Full Title: Prospective Randomized Evaluation of Emerging Novel Treatments for Infection prophylaxis in Total Joint Replacement (PREVENT-iT): A Pilot Study | ||
Medical condition: Persistent Draining Wound and Periprosthetic Joint Infection prevention in patients undergoing total joint replacement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005929-89 | Sponsor Protocol Number: CLOU064C12302 | Start Date*: 2022-02-01 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: A randomized, double-blind, double-dummy, parallel-group study, comparing the efficacy and safety of remibrutinib versus teriflunomide in participants with relapsing multiple sclerosis, followed by... | ||
Medical condition: Multiple Sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) IT (Trial now transitioned) FR (Trial now transitioned) GR (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) SI (Trial now transitioned) SK (Trial now transitioned) BG (Trial now transitioned) PL (Trial now transitioned) HR (Trial now transitioned) EE (Trial now transitioned) RO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002248-34 | Sponsor Protocol Number: FInCH | Start Date*: 2018-02-20 | |||||||||||||||||||||
Sponsor Name:King's College London | |||||||||||||||||||||||
Full Title: FInCH Study: A randomised feasibility study comparing fluoride interventions to prevent dental decay in older people in care homes. | |||||||||||||||||||||||
Medical condition: Prevention of dental decay in older people in care homes | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000641-23 | Sponsor Protocol Number: CNWL/MC/AFT/01 | Start Date*: 2015-11-24 |
Sponsor Name:Central and North West London NHS Foundation Trust | ||
Full Title: Aggression Following TBI: Effectiveness of Risperidone (AFTER)-a feasibility RCT. | ||
Medical condition: aggression and agitation following on from a traumatic brain injury | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002787-32 | Sponsor Protocol Number: RG_19-172 | Start Date*: 2020-11-16 |
Sponsor Name:University of Birmingham | ||
Full Title: Antidepressant for the prevention of DEPression following first episode Psychosis trial | ||
Medical condition: Patients with First Episode Psychosis. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000872-89 | Sponsor Protocol Number: MK001 | Start Date*: 2015-10-29 |
Sponsor Name:University of Oxford | ||
Full Title: ANODE: a randomised controlled trial of prophylactic ANtibiotics to investigate the prevention of infection following Operative vaginal DElivery. | ||
Medical condition: Maternal infection in the first six weeks after operative vaginal delivery. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004077-16 | Sponsor Protocol Number: 14/0249 | Start Date*: 2014-12-03 | |||||||||||
Sponsor Name:University College London Joint Research Office | |||||||||||||
Full Title: A Phase IV randomised controlled trial of the selective serotonin reuptake inhibitor Sertraline versus Cognitive Behavioural Therapy for anxiety symptoms in people with Generalised Anxiety Disorder... | |||||||||||||
Medical condition: Generalised anxiety disorder (GAD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003351-11 | Sponsor Protocol Number: GPRI-19102-TRA | Start Date*: 2019-12-19 |
Sponsor Name:GPRI | ||
Full Title: Triple therapy effectiveness in COPD patients with characteristics of asthma: A pragmatic Primary Care trial - The TRACkER trial | ||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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