- Trials with a EudraCT protocol (831)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
831 result(s) found for: covid-19.
Displaying page 9 of 42.
| EudraCT Number: 2021-006335-26 | Sponsor Protocol Number: Xe-long-COVID | Start Date*: 2022-03-04 | |||||||||||
| Sponsor Name:Aarhus University | |||||||||||||
| Full Title: Hyperpolarized xenon lung MRI in long-term COVID19 | |||||||||||||
| Medical condition: Long COVID19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003367-26 | Sponsor Protocol Number: MK4482-001 | Start Date*: 2020-11-18 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase 2/3, Randomized, Placebo-Controlled, Double-Blind Clinical Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of MK-4482 in Hospitalized Adults with COVID-19 | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) GB (GB - no longer in EU/EEA) SE (Completed) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001662-11 | Sponsor Protocol Number: CINC424J12301 | Start Date*: 2020-05-05 |
| Sponsor Name:Novartis Pharma AG | ||
| Full Title: Phase 3 randomized, double-blind, placebo-controlled, multi-center study to assess the efficacy and safety of ruxolitinib in patients with COVID-19 associated cytokine storm (RUXCOVID) | ||
| Medical condition: COVID-19 associated cytokine storm | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) FR (Completed) ES (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-000269-34 | Sponsor Protocol Number: GC2010 | Start Date*: 2021-03-20 | ||||||||||||||||||||||||||
| Sponsor Name:Grifols Therapeutics LLC | ||||||||||||||||||||||||||||
| Full Title: A Multicenter, Randomized, Double-blind, Parallel Group Study to Evaluate the Safety and Efficacy of Anti-COVID-19 Immune Globulin (Human) 20% (C19-IG 20%) versus Placebo in Asymptomatic Ambulatory... | ||||||||||||||||||||||||||||
| Medical condition: Subjects with laboratory-confirmed novel coronavirus (SARS-CoV-2) infection as determined by qualitative PCR (reverse transcriptase [RT]-PCR) that are asymptomathic | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2020-002102-58 | Sponsor Protocol Number: TJT2012 | Start Date*: 2020-06-12 | |||||||||||
| Sponsor Name:CHU de Liège | |||||||||||||
| Full Title: Mesenchymal stromal cell therapy for severe COVID-19 infection | |||||||||||||
| Medical condition: Patients with severe COVID-19 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001904-41 | Sponsor Protocol Number: GETAFIX-2020 | Start Date*: 2020-05-20 | |||||||||||
| Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
| Full Title: Glasgow Early Treatment Arm FavIpiravir : A randomized controlled study of favipiravir as an early treatment arm in COVID-19 patients | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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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: 2020-004323-16 | Sponsor Protocol Number: RCT-MP-COVID-19 | Start Date*: 2020-11-25 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA ARCISPEDALE SANTA MARIA NUOVA/IRCCS DI REGGIO EMILIA | |||||||||||||
| Full Title: A randomized, multicentre, double-blind study to evaluate the efficacy of high-dose administartion of methylprednisolone in addition to standard treatment, in SARS-CoV2 (COVID-19) pneumonia patients. | |||||||||||||
| Medical condition: COVID-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005395-35 | Sponsor Protocol Number: GatesMRI-COD-01-T01-01 | Start Date*: 2020-12-16 |
| Sponsor Name:Bill & Melinda Gates Medical Research Institute | ||
| Full Title: A randomized, controlled, Phase 2b study to evaluate safety and efficacy of rivaroxaban (Xarelto®) for high risk people with mild COVID-19 | ||
| Medical condition: Mild COVID-19 in people who are at high risk for moderate or severe disease due to age, body mass index (BMI) and comorbidities, many of which are also thrombotic risks. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-005526-29 | Sponsor Protocol Number: VP-VLY-686-3501 | Start Date*: 2021-03-31 | |||||||||||
| Sponsor Name:Vanda Pharmaceuticals Inc. | |||||||||||||
| Full Title: ODYSSEY: A randomized, double-blind, placebo-controlled study to investigate the efficacy of tradipitant in treating inflammatory lung injury and improving clinical outcomes associated with severe ... | |||||||||||||
| Medical condition: inflammatory lung injury associated with severe COVID-19 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001381-11 | Sponsor Protocol Number: APHP200409 | Start Date*: 2020-04-08 |
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
| Full Title: COVID-19 - ACE inhibitors or ARBs discontinuation for Clinical Outcome Risk reduction in patients hospitalized for the Endemic Severe acute respiratory syndrome coronavirus (SARS-CoV-2) infection: ... | ||
| Medical condition: Adult patients with a diagnosis of COVID-19 requiring hospitalization in a non-ICU and on prior therapy with RAS blockers | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-002120-37 | Sponsor Protocol Number: RESP301-002 | Start Date*: 2020-06-16 | |||||||||||
| Sponsor Name:Thirty Respiratory Limited | |||||||||||||
| Full Title: An open-label, adaptive randomized, controlled multicenter study to evaluate the efficacy and safety of RESP301 plus standard of care (SOC) compared to SOC alone in hospitalized participants with C... | |||||||||||||
| Medical condition: Coronavirus disease 2019 (COVID-19) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001634-36 | Sponsor Protocol Number: SARCOVID | Start Date*: 2020-04-09 |
| Sponsor Name:Rosario García de Vicuña | ||
| Full Title: Randomized open pilot study to evaluate the efficacy of subcutaneous sarilumab in patients with moderate-severe COVID-19 infection. | ||
| Medical condition: COVID-19 infection requiring hospitalization | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-001888-90 | Sponsor Protocol Number: 20201504 | Start Date*: 2020-04-30 | |||||||||||
| Sponsor Name:University of Southern Denmark | |||||||||||||
| Full Title: Using BCG vaccine to enhance non-specific protection of health care workers during the COVID-19 pandemic. A randomised controlled multi-center trial. | |||||||||||||
| Medical condition: Healthy volunteers, health care workers. Immune system activation after BCG vaccination. Work absenteeism and COVID-19 will be monitored. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001765-37 | Sponsor Protocol Number: PROTOCOLO/ICO/COVID20 | Start Date*: 2020-04-11 | ||||||||||||||||
| Sponsor Name:Institut Català d’Oncologia | ||||||||||||||||||
| Full Title: Pragmatic clinical trial to evaluate the efficacy of hydroxychloroquine in the treatment of COVID-19 infection in two cohorts: patients with oncohaematological disease and SARS-CoV-2 positive witho... | ||||||||||||||||||
| Medical condition: SAR COV2 virus infection, without radiological affectation. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-001937-11 | Sponsor Protocol Number: 132333 | Start Date*: 2020-04-30 |
| Sponsor Name:University College London | ||
| Full Title: A single-site, randomised, controlled, parallel design, open-label investigation of an approved nebulised recombinant human DNase enzyme (dornase alfa) to reduce hyperinflammation in hospitalised p... | ||
| Medical condition: Respiratory illness caused by Covid-19 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-003628-18 | Sponsor Protocol Number: 000000 | Start Date*: 2020-09-29 | ||||||||||||||||
| Sponsor Name:University of Oxford, Clinical Trials and Research Governance | ||||||||||||||||||
| Full Title: Adalimumab in COVID-19 to present respiratory failure in community care (AVID-CC): A randomised controlled trial | ||||||||||||||||||
| Medical condition: COVID-19 | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-001360-20 | Sponsor Protocol Number: MINECRAFT | Start Date*: 2021-07-29 | |||||||||||
| Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO | |||||||||||||
| Full Title: MINECRAFT Study: MINEralcorticoid receptor antagonism with CanRenone As eFfective Treatment in moderate to severe ARDS in COVID-19, a phase 2 clinical trial. | |||||||||||||
| Medical condition: SARS-CoV2 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-003363-25 | Sponsor Protocol Number: NA | Start Date*: 2020-08-18 | ||||||||||||||||
| Sponsor Name:Department of Intensive Care, Rigshospitalet | ||||||||||||||||||
| Full Title: Higher vs. Lower Doses of Dexamethasone in Patients with COVID-19 and Severe Hypoxia: the COVID STEROID 2 trial | ||||||||||||||||||
| Medical condition: Adult patients with COVID-19 and severe hypoxia. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-003779-17 | Sponsor Protocol Number: P2003GF | Start Date*: 2020-12-15 | |||||||||||
| Sponsor Name:G. Pohl-Boskamp GmbH & Co. KG | |||||||||||||
| Full Title: A clinical trial to assess the efficacy and safety of PB432 in COVID-19 positive inpatients with acute respiratory insufficiency (ARI) -COVARI- | |||||||||||||
| Medical condition: Covid-19 with acute respiratory insufficiency | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002730-16 | Sponsor Protocol Number: GLS27-005 | Start Date*: 2021-10-25 | |||||||||||
| Sponsor Name:GeneOne Life Science Inc. | |||||||||||||
| Full Title: Safety, Tolerability, Efficacy and Dose Response of GLS-1027 in the Prevention of Severe Pneumonitis caused by SARS-CoV-2 Infection | |||||||||||||
| Medical condition: Patients with SARS-CoV-2 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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