- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: Lateral flow test.
Displaying page 1 of 2.
EudraCT Number: 2016-002399-28 | Sponsor Protocol Number: RAP-ALS | Start Date*: 2017-07-14 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA POLICLINICO DI MODENA | |||||||||||||
Full Title: Rapamycin (Sirolimus) treatment for amyotrophic lateral sclerosis | |||||||||||||
Medical condition: definite or probable ALS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003479-20 | Sponsor Protocol Number: 2011/433 | Start Date*: 2013-04-15 | |||||||||||
Sponsor Name:Handkirurgiska kliniken, Universitetssjukhuset Örebro | |||||||||||||
Full Title: Lateral humerus epicondylitis- a clinical, muscle morpological, muscle metabolical and functional evaluation of a new model for treatment. | |||||||||||||
Medical condition: Chronic lateral humerus epiconcylitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001989-38 | Sponsor Protocol Number: IMCRELA | Start Date*: 2021-07-08 | |||||||||||
Sponsor Name:Facultad de medicina y ciencias de la salud de la Universidad Católica de Valencia | |||||||||||||
Full Title: IMPACT OF THE COMBINED TREATMENT OF THE LIPOSOMATED POLYPHENOLS CÚRCULA AND RESVERATROL® WITH DUTASTERIDE, IN THE CLINICAL IMPROVEMENT OF PATIENTS WITH ALS TREATED WITH RILUZOLE | |||||||||||||
Medical condition: Amyotrophic Lateral Sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
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: 2012-002742-20 | Sponsor Protocol Number: CL2-16257-101 | Start Date*: 2013-03-20 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Effect of ivabradine versus placebo on cardiac function, exercise capacity, and neuroendocrine activation in patients with Chronic Heart Failure with Preserved left ventricular Ejection Fraction A... | |||||||||||||
Medical condition: Heart failure with preserved left ventricular ejection fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PT (Completed) IT (Completed) DE (Completed) BE (Completed) GB (Completed) NL (Completed) ES (Completed) CZ (Completed) AT (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000805-27 | Sponsor Protocol Number: MEIN/10/Ran-Did/001 | Start Date*: 2012-10-23 | |||||||||||
Sponsor Name:Menarini International Operations Luxembourg S.A., Avenue de la Gare, 1611 Luxembourg, Luxembourg | |||||||||||||
Full Title: Effect of Ranolazine in Heart Failure Patients with Preserved Ejection Fraction | |||||||||||||
Medical condition: Heart failure patients with preserved ejection fraction (HFpEF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006340-60 | Sponsor Protocol Number: OPTUK RFCP PRO002.04 | Start Date*: 2007-03-14 |
Sponsor Name:OptiNose UK Ltd | ||
Full Title: A Double Blind, Randomised, Parallel Group, Placebo-Controlled Study to Investigate the Efficacy and Tolerability of Intranasal Fluticasone Propionate Delivered by the Optinose Device in Adult Pati... | ||
Medical condition: treatment of bilateral nasal polyposis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004132-22 | Sponsor Protocol Number: NPH-01 | Start Date*: 2021-01-20 | |||||||||||
Sponsor Name:Uppsala University Hospital | |||||||||||||
Full Title: Double-blind randomized acetazolamide trial in normal pressure hydrocephalus | |||||||||||||
Medical condition: Normal pressure hydrocephalus | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000655-36 | Sponsor Protocol Number: 80684 | Start Date*: 2023-04-06 |
Sponsor Name:Amsterdam UMC | ||
Full Title: Evaluation of GeranylGeranylAcetone in heart failure with preserved ejection fraction | ||
Medical condition: Heart Failure with preserved ejection fraction. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
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: 2022-002560-73 | Sponsor Protocol Number: SWITCH_ON | Start Date*: 2022-09-01 |
Sponsor Name:Erasmus MC | ||
Full Title: SWITCH ON: Analysing the immunogenicity of additional booster vaccinations in healthcare workers. | ||
Medical condition: To study the necessity to boost healthcare workers (which arre representative for the dutch population) with a COVID vaccin by measuring the immunogenicity at 7 days and 28 days.. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-006997-27 | Sponsor Protocol Number: CRAD001M2301 | Start Date*: 2011-06-01 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A randomized, double-blind, placebo-controlled study of RAD001 in the treatment of patients with subependymal giant cell astrocytomas (SEGA) associated with Tuberous Sclerosis Complex (TSC) | ||
Medical condition: This study will evaluate the antitumor activity of RAD001 versus placebo in patients with subependymal giant cell astrocytomas (SEGA) associated with Tuberous Sclerosis Complex (TSC). | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) IT (Completed) GB (Completed) DE (Completed) NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-022725-16 | Sponsor Protocol Number: RE-0240/2010/EN | Start Date*: 2012-03-30 | |||||||||||
Sponsor Name:FRANCISCO JOSE MORALES PONCE | |||||||||||||
Full Title: INTRACORONARY ADMINISTRATION OF TENECTEPLASE VERSUS ABCIXIMAB AS ADJUNCTIVE TREATMENT DURING PRIMARY ANGIOPLASTY IN ACUTE MYOCARDIAL INFARCTION OF ANTERIOR LOCATION | |||||||||||||
Medical condition: ACUTE MYOCARDIAL INFARCTION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004039-64 | Sponsor Protocol Number: MYK-461-007 | Start Date*: 2019-11-14 | |||||||||||
Sponsor Name:MyoKardia, Inc. | |||||||||||||
Full Title: A Long-term Safety Extension Study of Mavacamten (MYK-461) in Adults with Hypertrophic Cardiomyopathy Who Have Completed the MAVERICK-HCM (MYK-461-006) or EXPLORER-HCM (MYK-461-005) Trials (MAVA-LTE) | |||||||||||||
Medical condition: Hypertrophic Cardiomyopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PT (Trial now transitioned) CZ (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) PL (Trial now transitioned) DE (Trial now transitioned) DK (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018289-21 | Sponsor Protocol Number: EndoIGA2010 | Start Date*: 2010-02-25 | |||||||||||||||||||||||||||||||
Sponsor Name:Insitute of Endocrinology | |||||||||||||||||||||||||||||||||
Full Title: Clinical, laboratory and ultrasound markers for the prediction of the response on the pulse-dose treatment by intravenous glucocorticoids in patients with endocrine orbitopathy | |||||||||||||||||||||||||||||||||
Medical condition: active severe endocrine orbitopathy | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: CZ (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002530-17 | Sponsor Protocol Number: D7220C00001 | Start Date*: 2021-07-14 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II/III Partially Double-Blinded, Randomised, Multinational, Active-Controlled Study in Both Previously Vaccinated and Unvaccinated Adults to Determine the Safety and Immunogenicity of AZD28... | |||||||||||||
Medical condition: SARS-COV-2 infection (COVID-19) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001036-25 | Sponsor Protocol Number: UNI91103-201 | Start Date*: 2021-06-01 | |||||||||||
Sponsor Name:UNION therapeutics A/S | |||||||||||||
Full Title: A RANDOMIZED PLACEBO-CONTROLLED PHASE 2 STUDY TO ASSESS THE SAFETY AND EFFICACY OF UNI91103 INTRANASAL ADMINISTRATION IN ADULTS WITH ASYMPTOMATIC OR MILDLY SYMPTOMATIC COVID-19 | |||||||||||||
Medical condition: Covid-19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000641-33 | Sponsor Protocol Number: PAX | Start Date*: 2022-04-21 | |||||||||||
Sponsor Name:Fundació FLS de Lluita contra la Sida, les Malalties Infeccioses i la Promoció de la Salut i La Ciència | |||||||||||||
Full Title: Plasma Exchange Therapy for Post- COVID-19 Condition: A Pilot, Randomized Double-Blind Study | |||||||||||||
Medical condition: Post-Acute-Covid-19 Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000240-26 | Sponsor Protocol Number: PC_ASP_002 | Start Date*: 2019-05-17 | |||||||||||
Sponsor Name:Pulmocide Ltd | |||||||||||||
Full Title: An open-label, pilot study to assess safety, tolerability, pharmacokinetics and effects of inhaled PC945 in the pre-emptive treatment of Aspergillus fumigatus colonisation in lung transplant recipi... | |||||||||||||
Medical condition: Pre-emptive treatment of Aspergillus fumigatus colonisation in lung transplant recipients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000410-22 | Sponsor Protocol Number: U1111-1140-6242 | Start Date*: 2015-10-27 | ||||||||||||||||
Sponsor Name:The Cardiovascular MR Group, Dept. 2011, Rigshospitalet | ||||||||||||||||||
Full Title: Influence of liraglutide on diastolic cardiac function and myocardial perfusion as determined by magnetic resonance imaging in patients with type 2 diabetes: a double-blind randomized parallel-grou... | ||||||||||||||||||
Medical condition: Type 2 diabetes mellitus and diastolic heart faliure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
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