- Trials with a EudraCT protocol (281)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
		
	   		
	   		    
                    
                   	
                   	    281 result(s) found for: Hydroxychloroquine.
                    
                
			
   			
		
		Displaying page 1 of 15.
	
	
	| EudraCT Number: 2020-001697-30 | Sponsor Protocol Number: COVIDNA | Start Date*: 2020-04-23 | 
| Sponsor Name:NAVARRABIOMED - FUNDACIÓN MIGUEL SERVET | ||
| Full Title: PRE-EXPOSURE PROPHYLAXIS WITH HYDROXYCHLOROQUINE IN SANITARIES HIGHLY EXPOSED TO COVID-19. (COVIDNA) | ||
| Medical condition: PRE-EXPOSURE PROPHYLAXIS WITH HYDROXYCHLOROQUINE IN SANITARIES HIGHLY EXPOSED TO COVID-19 | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-003083-30 | Sponsor Protocol Number: PLAQHV | Start Date*: 2019-01-31 | |||||||||||
| Sponsor Name:UZ Leuven | |||||||||||||
| Full Title: The effect of hydroxychloroquine sulphate on hedonic food intake, appetite-related sensations and gastrointestinal hormone release in healthy female subjects | |||||||||||||
| Medical condition: The study is meant to have a better understanding in obesity and how we can prevent/cure it. Therefore, the product will first be tested in healthy, lean volunteers. | |||||||||||||
| 
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001434-35 | Sponsor Protocol Number: Hydroxycholoquin-COVID-19 | Start Date*: 2020-03-31 | 
| Sponsor Name:Cliniques universitaires Saint-Luc | ||
| Full Title: Monocentric Population Pharmacokinetic study of Hydroxychloroquine in COVID-19 Patients to inform its dosing optimization. | ||
| Medical condition: Subject tested positive for COVID-19 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001281-11 | Sponsor Protocol Number: 20CH065 | Start Date*: 2020-03-30 | ||||||||||||||||
| Sponsor Name:CHU de Saint Etienne | ||||||||||||||||||
| Full Title: Evaluation of the concentration/viral effect relationship of hydroxychloroquine in COVID-19 patients in the intensive care unit. | ||||||||||||||||||
| Medical condition: covid-19 | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-001421-31 | Sponsor Protocol Number: QUINAVID-19 | Start Date*: 2020-04-06 | |||||||||||
| Sponsor Name:Sociedad Española de Farmacia Hospitalaria | |||||||||||||
| Full Title: Clinical trial randomized, unblinded and controled for evaluation of efficacy and safety of hydroxychloroquine chemoprophylaxis against SARS-CoV-2 (COVID-19) infection in healthcare professionals. | |||||||||||||
| Medical condition: SARS-CoV-2 infection | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001357-52 | Sponsor Protocol Number: EnCovid-hidroxiCLOROQUINA | Start Date*: 2020-05-13 | |||||||||||
| Sponsor Name:IDIVAL | |||||||||||||
| Full Title: Randomized, Controlled, Double-blind Clinical Trial Comparing the Efficacy and Safety of Chemoprophylaxis With Hydroxychloroquine in Patients Under Biological Treatment and / or JAK Inhibitors in... | |||||||||||||
| Medical condition: Quimioprophylaxis of SARS-CoV-2 infection with hydroxyloquine (HCQ) in patients diagnosed with an immunomediated inflammatory disease who are following a treatment with biological agents and / or J... | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001565-37 | Sponsor Protocol Number: PrEP_COVID | Start Date*: 2020-04-03 | 
| Sponsor Name:ISGlobal | ||
| Full Title: PRE-EXPOSURE PROPHYLAXIS WITH HYDROXYCHLOROQUINE FOR HIGH-RISK HEALTHCARE WORKERS DURING THE COVID-19 PANDEMIC (PrEP_COVID): A UNICENTRIC, DOUBLE-BLINDED RANDOMIZED CONTROLLED TRIAL. | ||
| Medical condition: COVID-19 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001625-96 | Sponsor Protocol Number: PLAQOW | Start Date*: 2019-01-31 | |||||||||||
| Sponsor Name:UZ Leuven | |||||||||||||
| Full Title: The effect of hydroxychloroquine sulphate on hedonic food intake, appetite-related sensations and gastrointestinal hormone release in overweight female subject | |||||||||||||
| Medical condition: Obesity | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004866-86 | Sponsor Protocol Number: P160944J | Start Date*: 2020-01-23 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Evaluation of the benefit of adjuvant treatment with hydroxychloroquine to usual medical care for uncomplicated term pregnancy in patients with primary obstetrical antiphospholipid syndrome: random... | |||||||||||||
| Medical condition: Primary obstetrical antiphospholipid syndrome | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001441-39 | Sponsor Protocol Number: VIR20001 | Start Date*: 2020-05-12 | |||||||||||
| Sponsor Name:University of Oxford | |||||||||||||
| Full Title: Chloroquine/ hydroxychloroquine prevention of coronavirus disease (COVID-19) in the healthcare setting; a randomised, placebo-controlled prophylaxis study (COPCOV) | |||||||||||||
| Medical condition: COVID-19, acute respiratory illness | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001987-28 | Sponsor Protocol Number: PRECOV | Start Date*: 2020-05-06 | ||||||||||||||||
| Sponsor Name:OSPEDALE SAN RAFFAELE | ||||||||||||||||||
| Full Title: PRECOV: a randomized controlled clinical trial on the effects of hydroxychloroquine in the prevention of COVID-19 in healthcare workers at risk | ||||||||||||||||||
| Medical condition: Healthcare personnel at risk of SARS-CoV-2 infection | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-002449-41 | Sponsor Protocol Number: PRE-COVID | Start Date*: 2020-06-15 | |||||||||||
| Sponsor Name:ANTONIO ANTELA LOPEZ | |||||||||||||
| Full Title: Pilot trial on early treatment with hydroxychloroquine in patients with COVID-19 who do not have hospital admission at diagnosis. | |||||||||||||
| Medical condition: Patients diagnosed with COVID-19, with positive PCR for SARS-CoV-2, without criteria for hospital admission. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001333-13 | Sponsor Protocol Number: 20-37815010 | Start Date*: 2020-04-09 | 
| Sponsor Name:Groupe Hospitalier Paris Saint-Joseph | ||
| Full Title: Dexamethasone associated with hydroxychloroquine vs. hydroxychloroquine alone for the early treatment of severe ARDS caused by COVID-19 : a randomized controlled trial | ||
| Medical condition: Acute Respiratory Distress Syndrome (ARDS) caused by SARS-Cov-2 infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001257-51 | Sponsor Protocol Number: 220322020 | Start Date*: 2020-04-15 | |||||||||||||||||||||
| Sponsor Name:Rigshospitalet | |||||||||||||||||||||||
| Full Title: The Danish Pre-HCQ Dialysis Study: Hydroxychloroquine for prevention of COVID-19 in dialysis-treated patients with end-stage renal disease - A multicenter parallel-group open randomized clinical... | |||||||||||||||||||||||
| Medical condition: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) | |||||||||||||||||||||||
| 
 | |||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2010-019684-11 | Sponsor Protocol Number: 2010-WL01 | Start Date*: 2010-06-09 | |||||||||||
| Sponsor Name:Maasstad Hospital | |||||||||||||
| Full Title: Pharmacological Treatment in Osteoarthritis | |||||||||||||
| Medical condition: Osteoarthritis of the hand | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-007056-18 | Sponsor Protocol Number: 3403 | Start Date*: 2007-03-16 | |||||||||||
| Sponsor Name:The Newcastle upon tyne Hospitals NHS Trust | |||||||||||||
| Full Title: The Discoid Lupus Research Project | |||||||||||||
| Medical condition: Discoid lupus erythematosus | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012499-28 | Sponsor Protocol Number: HLS01/2009 | Start Date*: 2009-08-07 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
| Full Title: Efficacy of the treatment with hydroxychloroquine in non responders HIV-infected HAART-treated patients | |||||||||||||
| Medical condition: HIV infection (immunological nonresponders). | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000233-73 | Sponsor Protocol Number: HCQvJan11 | Start Date*: 2016-01-05 | 
| Sponsor Name:Helsinki University Central Hospital | ||
| Full Title: HYDROXYCHLOROQUINE IN ACUTE CORONARY SYNDROME: PREVENTION OF RECURRENT CARDIOVASCULAR EVENTS | ||
| Medical condition: Cardiovascular disease | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001512-26 | Sponsor Protocol Number: COMIHY | Start Date*: 2020-04-22 | |||||||||||
| Sponsor Name:Universitätsklinikum Tübingen | |||||||||||||
| Full Title: Hydroxychloroquine for the treatment of mild COVID-19 disease | |||||||||||||
| Medical condition: Acute coronavirus disease 2019 | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001265-36 | Sponsor Protocol Number: UCDCRC/20/01 | Start Date*: 2020-05-05 | |||||||||||
| Sponsor Name:University College Dublin | |||||||||||||
| Full Title: A multicentre, prospective, randomised trial comparing standard of care (SOC) alone, SOC plus hydroxychloroquine monotherapy or SOC plus a combination of hydroxychloroquine and azithromycin in the ... | |||||||||||||
| Medical condition: SARS-CoV-2 PCR-positive population | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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