- Trials with a EudraCT protocol (505)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
505 result(s) found for: Sample size.
Displaying page 1 of 26.
EudraCT Number: 2013-005430-37 | Sponsor Protocol Number: | Start Date*: 2015-01-02 | |||||||||||
Sponsor Name:North Bristol NHS Trust | |||||||||||||
Full Title: Use of co-trimoxazole to prevent pneumonia in patients with severe head injury | |||||||||||||
Medical condition: Pneumonia secondary to severe head injury. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002724-17 | Sponsor Protocol Number: 02-NDOL-006 | Start Date*: 2005-04-19 |
Sponsor Name:Fresenius Kabi Deutschland GmbH | ||
Full Title: Efficacy of Neodolpasse™ in the treatment of postoperative pain: Morphine sparing effect during the first 24 hours postoperatively after unilateral total hip arthroplasty. | ||
Medical condition: Patients with ASA classification I-III, female or male between 18 and 85 years of age, undergoing primary cementless unilateral total hip arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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: 2021-000827-11 | Sponsor Protocol Number: T50/2021 | Start Date*: 2022-09-02 |
Sponsor Name:Turku University Hospital | ||
Full Title: Clinical use of USPIO contrast media in the assessment of pelvic lymph node metastasis in rectal cancer. | ||
Medical condition: Pelvic lymph node metastasis in rectal cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001772-20 | Sponsor Protocol Number: CMR001/05 | Start Date*: 2007-03-15 |
Sponsor Name:Clinica Rotger | ||
Full Title: Effect of intracoronary injection of autologous stemm cells on left ventricular ejection fraction and volumes one year after an acute myocardial infarction. Efecto de la inyección intracoronaria d... | ||
Medical condition: The trial evaluates the effect on left ventricular function recovery of the intracoronary injection of mononuclear white cells obtained from peripheral blood in the week after an acute myocardial i... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000294-78 | Sponsor Protocol Number: CTP001H | Start Date*: 2019-06-07 |
Sponsor Name:Nektr Technologies | ||
Full Title: A Randomized, Single-Blinded, Comparative Study of Mycosinate and Curanail in the Treatment of Fungal Nail Infection | ||
Medical condition: Onychomycosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-000573-72 | Sponsor Protocol Number: ATOS-010 | Start Date*: 2018-04-21 |
Sponsor Name:Atossa Genetics Inc | ||
Full Title: Karma CREME-1: A double-blind, placebo-controlled, three-armed, pilot study of the effects, safety and tolerability of topical endoxifen in women within the Karma Cohort | ||
Medical condition: The mammographic density reduction in healthy women. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000349-30 | Sponsor Protocol Number: NL60669 | Start Date*: 2017-08-02 |
Sponsor Name:Academic Medical Center | ||
Full Title: Effect of INtervention with DMR, GLP-1 and lifestyle intensification -in Subjects with insulin dePendent type 2 diabetes- on Insulin Requirement and mEtabolic parameters | ||
Medical condition: Type 2 diabetes mellitus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002063-14 | Sponsor Protocol Number: GEMCAD-1402 | Start Date*: 2014-10-23 | |||||||||||
Sponsor Name:GEMCAD (Grupo Español Multidisciplinar en Cáncer Digestivo) | |||||||||||||
Full Title: Induction FOLFOX with or without Aflibercept followed by chemoradiation in High Risk Locally Advanced Rectal Cancer. Phase II randomized, multicenter, open label trial | |||||||||||||
Medical condition: Patients with high risk locally advanced rectal carcinoma (defined by Magnetic Resonance Imaging [MRI]), who are candidates for multimodality treatment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001240-21 | Sponsor Protocol Number: 69024 | Start Date*: 2019-07-03 |
Sponsor Name:Amsterdam UMC, location AMC | ||
Full Title: Exposure to orally administered antibiotics during the initial phase of infection in non-critically ill, febrile patients | ||
Medical condition: Exposure to oral antibiotics will be investigated in infectious patients when they are febrile compared to when they are afebrile. The infection itself is unspecified. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000591-34 | Sponsor Protocol Number: 123456 | Start Date*: 2011-05-06 |
Sponsor Name:Mater University Hospital | ||
Full Title: SIRS Steroids In caRdiac Surgery Trial | ||
Medical condition: Study Objective(s) To determine whether high-risk patients undergoing cardiac surgery requiring CPB derive benefit from perioperative steroids. Study Design Multicentre, International, random... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003451-34 | Sponsor Protocol Number: intrusion | Start Date*: 2023-05-03 |
Sponsor Name:Erasmus Medical Center | ||
Full Title: INTRUSION: Unraveling the INTRatUmoral PK/PD relatION for SAR408701 | ||
Medical condition: metastatic non-squamous non-small cell lung cancer metastatic estrogen positive breast cancer metastatic gastric cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006953-77 | Sponsor Protocol Number: 27-12-2021 | Start Date*: 2022-04-11 | ||||||||||||||||||||||||||
Sponsor Name:Aarhus University Hospital | ||||||||||||||||||||||||||||
Full Title: Treatment effects of Bisoprolol and Verapamil in symptomatic patients with non-obstructive hypertrophic cardiomyopathy | ||||||||||||||||||||||||||||
Medical condition: Non-obstructive Hypertrophic cardiomyopathy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001498-63 | Sponsor Protocol Number: BIO101-CL05 | Start Date*: 2020-07-22 | ||||||||||||||||
Sponsor Name:Biophytis S.A. | ||||||||||||||||||
Full Title: Adaptive design phase 2 to 3, randomized, double- blind, multicenter, to evaluate the safety, efficacy, pharmacokinetics and pharmacodynamics of BIO101 in the prevention of the respiratory deterior... | ||||||||||||||||||
Medical condition: Confirmed infection with SARS-CoV-2 (COVID-19) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) BE (Completed) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000784-16 | Sponsor Protocol Number: NCPACI | Start Date*: 2016-04-15 |
Sponsor Name:Akershus University Hospital | ||
Full Title: Focal cartilage defects in the knee – A randomized controlled trial comparing Autologous Chondrocyte Implantation with arthroscopic debridement | ||
Medical condition: Symptomatic focal cartilage defects in the knee | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004093-27 | Sponsor Protocol Number: ML20493 | Start Date*: 2007-04-04 | |||||||||||
Sponsor Name:Roche (Hungary) Ltd. | |||||||||||||
Full Title: A multicenter, phase II, open-label study evaluating the benefit of addition of MabThera (rituximab) to standard chemotherapies in patients with previously untreated mantle cell lymphoma. | |||||||||||||
Medical condition: Mantle cell lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005125-11 | Sponsor Protocol Number: RCT-EPO-001 | Start Date*: 2008-12-19 | |||||||||||
Sponsor Name:Walton Centre for Neurology and Neurosurgery | |||||||||||||
Full Title: A pilot single-centre randomised controlled trial of recombinant human erythropoietin versus placebo in primary progressive multiple sclerosis. | |||||||||||||
Medical condition: Primary progressive multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001097-27 | Sponsor Protocol Number: MONO-01 | Start Date*: 2005-09-29 |
Sponsor Name:Bio-Gels Pharmaceuticals | ||
Full Title: A Study of the Clinical Activity of Monocaprin/Doxycycline Gel on Cold Sores | ||
Medical condition: Herpes simplex virus (HSV) has plagued mankind worldwide for thousands of years. Once HSV enters the body, it penetrates vulnerable cells in the lower layers of human skin tissue and replicates its... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002360-14 | Sponsor Protocol Number: AK-2016-HHC1 | Start Date*: 2016-09-29 | ||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet, Dapartment of of Clinical Physiology, Nuclear Medicine and PET | ||||||||||||||||||||||||||||
Full Title: Phase II trial: PET/CT for staging advanced and localized oral and oropharyngeal cancer | ||||||||||||||||||||||||||||
Medical condition: Oral squamous cell cancer (OSCC) with and with out local metastasis Oropharyngeal squamous cell cancer (OPSCC) with and with out local metastasis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003883-20 | Sponsor Protocol Number: CSTI571JDE74 | Start Date*: 2008-09-30 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: An open-label, multicenter, expanded access study of imatinib mesylate in adult patients with GIST in adjuvant setting after R0-resection | |||||||||||||
Medical condition: gastrointestinal stromal tumors - adjuvant treatment after surgical tumor resection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) FR (Completed) IT (Completed) SK (Completed) CZ (Completed) BE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
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