- Trials with a EudraCT protocol (141)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
141 result(s) found for: Meaning.
Displaying page 1 of 8.
EudraCT Number: 2017-003124-73 | Sponsor Protocol Number: na | Start Date*: 2018-01-31 |
Sponsor Name:Maastricht University | ||
Full Title: Carnitine supplementation as a therapy to improve insulin sensitivity in Type 2 diabetic patients with low carnitine status | ||
Medical condition: Glucose tolerance | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003985-40 | Sponsor Protocol Number: CZOL446G2422 | Start Date*: 2006-01-09 |
Sponsor Name:Department of Internal Medicine, University Hospital Gasthuisberg | ||
Full Title: A prospective multicentre phase II trial of zoledronic acid in patients with myelofibrosis with myeloid metaplasia (MMM) | ||
Medical condition: myelofibrosis with myeloid metaplasia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) ES (Completed) DE (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005673-60 | Sponsor Protocol Number: Droxidopa-302 | Start Date*: 2009-04-22 |
Sponsor Name:Chelsea Therapeutics Inc | ||
Full Title: A MULTI-CENTER, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP WITHDRAWAL-DESIGN STUDY TO ASSESS THE CLINICAL EFFECT OF DROXIDOPA IN SUBJECTS WITH PRIMARY AUTONOMIC FAILURE, DOPAMINE ... | ||
Medical condition: Symptomatic neurogenic orthostatic hypotension (NOH) in patients with Primary Autonomic Failure (PD, MSA and PAF), DBH deficiency and Non-Diabetic Neuropathy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001417-18 | Sponsor Protocol Number: DTS-301CLI001 | Start Date*: 2005-09-27 |
Sponsor Name:DIATOS S.A. | ||
Full Title: A Phase II Clinical Trial to Evaluate Intratumoral Injection of a Depot Formulation of Paclitaxel (DTS-301) as Neoadjuvant Therapy of Patients with Breast Cancer | ||
Medical condition: Invasive primary breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Prematurely Ended) HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001306-87 | Sponsor Protocol Number: CANc/CHF14/TIF | Start Date*: 2005-06-13 | |||||||||||
Sponsor Name:TAKEDA | |||||||||||||
Full Title: EFFECTS OF CANDESARTAN CILEXETIL VS STANDARD THERAPY ON SERUM LEVELS OF BRAIN NATRIURETIC PEPTIDE IN PATIENTS SUFFERING FROM CHRONIC HEART FAILURE WITH DEPRESSED AND PRESERVED SYSTOLIC FUNCTION | |||||||||||||
Medical condition: CHRONIC HEART FAILURE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003746-42 | Sponsor Protocol Number: om 145 | Start Date*: 2003-02-11 | |||||||||||
Sponsor Name:OSPEDALE ONCOLOGICO DI BARI | |||||||||||||
Full Title: Immunotherapy vs immuno-chemotherapy in patients with metastatic kidney carcinoma | |||||||||||||
Medical condition: metastatic kidney carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005285-38 | Sponsor Protocol Number: GM-IMAB-001-03 | Start Date*: 2012-05-09 | |||||||||||||||||||||
Sponsor Name:Astellas Pharma Global Development Inc. | |||||||||||||||||||||||
Full Title: A randomized Phase II multicenter, Open Label Study Evaluating the Efficacy and Safety of IMAB362 in Combination with the EOX (Epirubicin, Oxaliplatin, Capecitabine) regimen as First-Line Treatmen... | |||||||||||||||||||||||
Medical condition: advanced adenocarcinoma of the stomach, the esophagus or the gastroesophageal junction | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) CZ (Prematurely Ended) LV (Prematurely Ended) BG (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003533-41 | Sponsor Protocol Number: 1241.20 | Start Date*: 2012-12-04 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: A Phase III, Randomised, Partially Double-Blind and Placebo-Controlled Study of BI 207127 in Combination with Faldaprevir and Ribavirin in Treatment-Naïve Patients with Chronic Genotype 1 HCV Infec... | |||||||||||||
Medical condition: Chronic infection with HCV - genotype 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PT (Completed) GB (Completed) ES (Completed) IE (Completed) IT (Completed) NL (Completed) HU (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003176-38 | Sponsor Protocol Number: 135.312 | Start Date*: 2006-05-22 |
Sponsor Name:Boehringer Ingelheim Pharma Ges mbH | ||
Full Title: A placebo controlled trial of alteplase (rt-PA) in acute ischemic hemispheric stroke where thrombolysis is initiated between 3 and 4 hours 30 minutes after stroke onset | ||
Medical condition: Ischemic stroke 3 and 4 hours 30 minutes before treatment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) SK (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002386-18 | Sponsor Protocol Number: 11-185/CAIAC | Start Date*: 2016-03-15 |
Sponsor Name:RWTH Aachen Clinical Trials Center Aachen (CTC-A) | ||
Full Title: Network connectivity and inhibitory control under atomoxetin challenge - A pharamacological "resting state" and "inhibitory task" fMRI study in patients with ADHD | ||
Medical condition: Patients with Attention-Deficit/Hyperactivity Disorders (ADHD) | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-003777-63 | Sponsor Protocol Number: 202100482 | Start Date*: Information not available in EudraCT |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Tetrahydrobiopterin (BH4) treatment in Phenylketonuria - comparing different practices of dosing regimen | ||
Medical condition: Phenylketonuria (PKU; OMIM 261600) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000310-15 | Sponsor Protocol Number: HC-MRI-GBM | Start Date*: 2020-03-26 | |||||||||||
Sponsor Name:Christoffer Laustsen | |||||||||||||
Full Title: MRI WITH HYPERPOLARISED PYRUVATE IN GLIOBLASTOMA – A PHASE II STUDY | |||||||||||||
Medical condition: Glioblastoma multiforme | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004711-39 | Sponsor Protocol Number: 2017-11-10 | Start Date*: 2018-04-10 | |||||||||||
Sponsor Name:Merja Kokki | |||||||||||||
Full Title: Tramadol-paracetamol in spine surgery | |||||||||||||
Medical condition: Postoperative pain after spine surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001924-11 | Sponsor Protocol Number: 37/2007/O/Sper | Start Date*: 2007-06-05 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Primary fungal profilaxis with Liposomal Amphotericin B at the dose of 10 mg/kg a week in adult patient undergoing orthotopic liver transplantation and high risk for postoperative fungal infection:... | |||||||||||||
Medical condition: Postoperative fungal infection. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004853-26 | Sponsor Protocol Number: T315/2018 | Start Date*: 2019-03-25 | ||||||||||||||||
Sponsor Name:Turku University Hospital | ||||||||||||||||||
Full Title: The effect of androgen deprivation therapy on the expression of prostate specific membrane antigen (PSMA) in treatment naive metastatic prostate cancer | ||||||||||||||||||
Medical condition: Metastatic prostate cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: FI (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000023-33 | Sponsor Protocol Number: PIR-BO-11-001 | Start Date*: 2011-11-02 | |||||||||||
Sponsor Name:S.P.A. ITALIANA LABORATORI BOUTY | |||||||||||||
Full Title: Clinical trial to evaluate, in patient suffering of neck pain the therapeutic equivalence, tolerability and satisfaction of subjects treated by medicated plaster containing piroxicam or diclofenac. | |||||||||||||
Medical condition: cervical pain of osteoarthritic origin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001889-16 | Sponsor Protocol Number: CLB-2006 | Start Date*: 2006-03-01 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
Full Title: Use of clembuterol in patients affected by valvular hearth disease and dilated cardiomyopathy | |||||||||||||
Medical condition: No healthy subjects (patients affected by valvular hearth disease and dilated cardiomyopathy) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000383-88 | Sponsor Protocol Number: CSC/Keto-01/06 | Start Date*: 2006-06-19 | |||||||||||
Sponsor Name:CSC Pharmaceuticals Handels GmbH | |||||||||||||
Full Title: A Multicenter, Parallel-group, Double-blind, Placebo Controlled and Randomized Clinical Study to Assess the Efficacy and Safety of Ketoprofen 10% Cutaneous Spray versus Placebo in Patients with Acu... | |||||||||||||
Medical condition: Painful, acute ankle sprains, as a model of general traumatic soft-tissue injuries | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001613-33 | Sponsor Protocol Number: BRIDGE | Start Date*: 2014-05-13 | ||||||||||||||||
Sponsor Name:Thoraxclinic at the University of Heidelberg | ||||||||||||||||||
Full Title: Iloprost for Bridging to Heart Transplantation in Patients with Pulmonary Hypertension and Left Heart Failure | ||||||||||||||||||
Medical condition: Pulmonary Hypertension and Left Heart Failure | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003822-96 | Sponsor Protocol Number: AC-055G201 | Start Date*: 2014-05-08 | ||||||||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd. | ||||||||||||||||||
Full Title: A prospective, multicenter, double-blind, randomized, placebo-controlled, parallel group, 12-week study to evaluate the safety and tolerability of macitentan in subjects with combined pre- and post... | ||||||||||||||||||
Medical condition: Combined pre- and post-capillary pulmonary hypertension (CpcPH) due to left ventricular dysfunction. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) CZ (Completed) AT (Completed) BE (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
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