- Trials with a EudraCT protocol (23)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
23 result(s) found for: Randomized Block Design.
Displaying page 1 of 2.
EudraCT Number: 2015-003987-35 | Sponsor Protocol Number: Metamizole001 | Start Date*: 2015-11-10 |
Sponsor Name:JESSA Hospital | ||
Full Title: Metamizole versus NSAID at home after ambulatory surgery: a double-blind randomized controlled trial | ||
Medical condition: Pain after ambulatory surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004866-27 | Sponsor Protocol Number: SAS105519 | Start Date*: 2016-08-03 |
Sponsor Name:GlaxoSmithKline Research & Development | ||
Full Title: A repeat-dose, open-label, randomized, incomplete block design in pediatric subjects with asthma, ages 4 - 11 years, to compare systemic exposure and pharmacodynamics of fluticasone propionate and ... | ||
Medical condition: Asthma | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2006-000313-38 | Sponsor Protocol Number: EFC5965 | Start Date*: 2007-01-24 | |||||||||||
Sponsor Name:Sanofi-aventis Recherche & Développement | |||||||||||||
Full Title: Randomized, multinational, double-blind study, comparing a high loading dose regimen of clopidogrel versus standard dose in patients with unstable angina or myocardial infarction managed with an ea... | |||||||||||||
Medical condition: Patients with non-ST segment elevation myocardial infarction managed with an early PCI. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) FI (Completed) IE (Completed) SK (Completed) FR (Completed) SE (Completed) DE (Completed) AT (Completed) EE (Completed) BG (Completed) GR (Completed) IT (Completed) GB (Completed) LT (Completed) NL (Completed) LV (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003973-23 | Sponsor Protocol Number: 213831 | Start Date*: 2021-06-29 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd. | |||||||||||||
Full Title: A Randomized Phase 3 Double-Blinded Study Comparing the Efficacy and Safety of Niraparib to Placebo in Participants with Either HER2-Negative BRCA-Mutated or Triple-Negative Breast Cancer with Mole... | |||||||||||||
Medical condition: Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) IE (Ongoing) PL (Ongoing) NL (Ongoing) FI (Completed) BE (Ongoing) DE (Completed) IT (Prematurely Ended) ES (Ongoing) HU (Completed) PT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005442-20 | Sponsor Protocol Number: E2020-G000-334 | Start Date*: 2008-09-04 |
Sponsor Name:Eisai Limited | ||
Full Title: Randomized, Double-Blind, Placebo-Controlled Study of Efficacy and Safety of Donepezil Hydrochloride in Preadolescent and Adolescent Children with Attention Impairment Following Cancer Treatment | ||
Medical condition: Attention impairment after cancer treatment | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) BE (Completed) ES (Completed) FR (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005435-28 | Sponsor Protocol Number: E2020-G000-333 | Start Date*: 2008-09-03 |
Sponsor Name:Eisai Limited | ||
Full Title: Randomized, Double-Blind, Placebo-Controlled Study of Efficacy and Safety of Donepezil Hydrochloride in Preadolescent and Adolescent Children with Attention Impairment Following Cancer Treatment | ||
Medical condition: Attention impairment after cancer treatment | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) NL (Completed) FR (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002255-42 | Sponsor Protocol Number: MK-3222-010 | Start Date*: 2013-01-10 | |||||||||||
Sponsor Name:Sun Pharma Global FZE | |||||||||||||
Full Title: A 64-Week, Phase 3, Randomized, Placebo-Controlled, Parallel Design Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous Tildrakizumab (SCH 900222/MK-3222), Followed by an Optiona... | |||||||||||||
Medical condition: Moderate-to-Severe Chronic Plaque Psoriasis | |||||||||||||
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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: 2019-003084-21 | Sponsor Protocol Number: cHL-PG01 | Start Date*: 2020-01-13 | |||||||||||
Sponsor Name:PROF.BRUNANGELO FALINI, DR.ENRICO TIACCI. DIPARTIMENTO DI MEDICINA, UNIVERSITA' DI PERUGIA | |||||||||||||
Full Title: A phase-II academic trial testing, in two parallel non-randomized cohorts, the combination of ruxolitinib (JAK1/2 inhibitor) with brentuximab or nivolumab in relapsed or refractory classical Hodgki... | |||||||||||||
Medical condition: Patients with relapsed or refractory cHL that has not responded to, or has progressed after, the previous treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001377-88 | Sponsor Protocol Number: MK-3222-011 | Start Date*: 2013-06-04 | |||||||||||
Sponsor Name:Sun Pharma Global FZE | |||||||||||||
Full Title: A 52-Week, Phase 3, Randomized, Active Comparator and Placebo-Controlled, Parallel Design Study to Evaluate the Efficacy and Safety/Tolerability of Subcutaneous Tildrakizumab (SCH 900222 / MK-3222)... | |||||||||||||
Medical condition: Moderate-to-Severe Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) AT (Completed) BE (Completed) CZ (Completed) IT (Completed) NL (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001996-33 | Sponsor Protocol Number: CD12_COVID-19 | Start Date*: 2020-08-26 | |||||||||||
Sponsor Name:CytoDyn, Inc. | |||||||||||||
Full Title: A Phase 2b/3, Randomized, Double Blind, Placebo Controlled, Adaptive Design Study to Evaluate the Efficacy and Safety of Leronlimab for Patients with Severe or Critical Coronavirus Disease 2019 (CO... | |||||||||||||
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: (No results available) |
EudraCT Number: 2014-003498-41 | Sponsor Protocol Number: D-Fampr | Start Date*: 2015-09-22 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Effects of dalfampridine on mobility in the context of daily life | ||
Medical condition: Motor behaviour and cognition in multiple sclerosis patients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001167-12 | Sponsor Protocol Number: IMMUNED | Start Date*: 2015-05-21 | |||||||||||
Sponsor Name:University of Essen | |||||||||||||
Full Title: A Phase II Randomized, Double-Blind Trial of Immunotherapy with Nivolumab or Nivolumab plus Ipilimumab versus Double-Placebo Control as a Post-Surgical/Post-Radiation Treatment for Stage IV Melanom... | |||||||||||||
Medical condition: Stage IV melanoma with no evidence of disease after surgery or radiotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002211-10 | Sponsor Protocol Number: GRASPA-TNBC-2018-02 | Start Date*: 2019-03-20 | |||||||||||
Sponsor Name:ERYTECH Pharma | |||||||||||||
Full Title: A Randomized Phase 2/3 Study of Eryaspase in Combination with Gemcitabine and Carboplatin Chemotherapy versus Chemotherapy Alone for the Treatment of Patients with Metastatic or Locally Recurrent T... | |||||||||||||
Medical condition: Triple-Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022365-10 | Sponsor Protocol Number: ARQ197-A-U302 | Start Date*: 2011-02-11 | ||||||||||||||||
Sponsor Name:Daiichi Sankyo Development Limited | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Double-Blinded, Placebo-Controlled Study of ARQ 197 Plus Erlotinib Versus Placebo Plus Erlotinib in Previously Treated Subjects with Locally Advanced or Metastatic, Non-Squam... | ||||||||||||||||||
Medical condition: Non-squamous, non–small-cell lung cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) CZ (Completed) DE (Completed) ES (Completed) IT (Completed) SE (Completed) GB (Completed) DK (Completed) AT (Completed) BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001810-32 | Sponsor Protocol Number: EP-101-03 | Start Date*: 2011-08-23 | |||||||||||
Sponsor Name:Elevation Pharmaceuticals, Inc | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Seven Arm, Four-Period Cross-over, Incomplete Block Design, 7-Day Dosing Study to Assess the Dose-Response, Safety, and Efficacy of EP-... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001500-41 | Sponsor Protocol Number: COV-AID | Start Date*: 2020-04-03 |
Sponsor Name:University Hospital Ghent | ||
Full Title: A prospective, randomized, factorial design, interventional study to compare the safety and efficacy of combinations of blockade of interleukin-6 pathway and interleukin-1 pathway to best standard ... | ||
Medical condition: COVID-19 patients with acute hypoxic respiratory failure and systemic cytokine release syndrome. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000705-20 | Sponsor Protocol Number: EsPhALL2017/COGAALL1631 | Start Date*: 2017-12-11 | ||||||||||||||||
Sponsor Name:Università degli Studi Milano Bicocca | ||||||||||||||||||
Full Title: International phase 3 trial in Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) testing imatinib in combination with two different cytotoxic chemotherapy backbones | ||||||||||||||||||
Medical condition: Philadelphia positive Acute Lumphoblastic Leukemia | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Ongoing) IT (Ongoing) NL (Ongoing) CZ (Ongoing) DE (Ongoing) FI (Ongoing) BE (Ongoing) SE (Ongoing) PL (Ongoing) DK (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004534-28 | Sponsor Protocol Number: Hyp1-18/2016 | Start Date*: 2018-08-09 | |||||||||||
Sponsor Name:Dr. August Wolff GmbH & Co. KG Arzneimittel | |||||||||||||
Full Title: Combined Randomized, Double-Blind, Dose-Confirming Phase 3a Study in Parallel Design to Assess the Efficacy and Safety of Topical 4-Week Treatment With 1% GPB Cream vs Placebo and Open-Label Phase... | |||||||||||||
Medical condition: Severe primary axillary hyperhidrosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) HU (Completed) DK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000567-26 | Sponsor Protocol Number: 2010-021883-14 | Start Date*: 2013-01-31 | |||||||||||
Sponsor Name:Radboud University Medical Centre Nijmegen | |||||||||||||
Full Title: A randomized double-blind, placebo-controlled study of risperidone in the treatment of DSM-IV-TR conduct disorder in children and adolescents. | |||||||||||||
Medical condition: Conduct Disorder DSM-IV-TR; 312.8x¸ APA, 2000 | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Ongoing) GB (GB - no longer in EU/EEA) ES (Ongoing) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021884-34 | Sponsor Protocol Number: PERS3 | Start Date*: 2013-01-24 | |||||||||||
Sponsor Name:Radboud University Medical Centre Nijmegen | |||||||||||||
Full Title: Relapse prevention in children and adolescents with DSM-IV Conduct Disorder treated with Risperidone: a Randomized Double blind, Placebo-Controlled, Discontinuation Study. | |||||||||||||
Medical condition: Conduct Disorder DSM-IV-TR; 312.8x, APA 2000 | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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