- Trials with a EudraCT protocol (39,286)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
39,286 result(s) found for: $1.
Displaying page 1,491 of 1,965.
EudraCT Number: 2006-001491-21 | Sponsor Protocol Number: 1-2006 | Start Date*: Information not available in EudraCT |
Sponsor Name:Max Planck Institute of Psychiatry | ||
Full Title: Studies on Permeability of the Blood-Brain-Barrier for Escitaloprame related to various Genotypes of the ABCB1-Gene: Effects on Sleep and Motoric Learning | ||
Medical condition: Effects on sleep electroencephalogram and motoric learning in healthy volunteers related to the permeability of the blood-brain-barrier related to genotypes of the ABCB 1 gene | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002791-14 | Sponsor Protocol Number: 1707-CL-0011 | Start Date*: 2013-02-14 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Phase 2 Study to Assess the Efficacy, Safety, and Dose-Response Relationship of ASP1707 in Subjects with Endometriosis Associated Pelvic Pain for 12 ... | |||||||||||||
Medical condition: endometriosis associated pelvic pain | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) GB (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024665-52 | Sponsor Protocol Number: AMSC-DSD-001 | Start Date*: 2013-07-24 | |||||||||||
Sponsor Name:Bioinova, s.r.o. | |||||||||||||
Full Title: Utilization of Autologous Mesenchymal Cells in Posterolateral Spinal Fusion in Degenerative Spine Disease: a Prospective, Non-randomized, Open-Label Study to Assess the Safety and the Efficacy. | |||||||||||||
Medical condition: Spinal degenerative disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022695-31 | Sponsor Protocol Number: 20110204 | Start Date*: 2011-04-12 | ||||||||||||||||
Sponsor Name:Karolinska Institute, Södersjukhuset AB | ||||||||||||||||||
Full Title: Effects on subclinical heartfailure in type 2 diabetic subjects on liraglutide treatment versus glimepiride both in combination with metformin. | ||||||||||||||||||
Medical condition: Type 2 diabetes mellitus and sublinical heart failure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020106-15 | Sponsor Protocol Number: SPAREIII | Start Date*: 2010-10-07 |
Sponsor Name:Fundació Clinic per la Recerca Biomédica | ||
Full Title: Estudio español de fibrilación auricular y resincronización | ||
Medical condition: FIBRILACIÓN AURICULAR Y RESINCRONIZACIÓN | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005094-54 | Sponsor Protocol Number: TPI ASM8-205 | Start Date*: 2008-01-17 | ||||||||||||||||
Sponsor Name:Topigen Pharmaceuticals Inc. | ||||||||||||||||||
Full Title: A MULTICENTER, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, CROSSOVER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF 14-DAY INHALED TPI ASM8 IN SUBJECTS WITH ASTHMA | ||||||||||||||||||
Medical condition: allergic asthma and allergen-induced asthma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007805-58 | Sponsor Protocol Number: KP-MSD-01-08 | Start Date*: 2009-11-16 | ||||||||||||||||||||||||||
Sponsor Name:Med. Klinik II, Grosshadern, Klinikum der Universität München | ||||||||||||||||||||||||||||
Full Title: The effect of sitagliptin on postprandial lipoprotein metabolism in patients with diabetes mellitus type 2 | ||||||||||||||||||||||||||||
Medical condition: Diabetes mellitus type 2 | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000213-19 | Sponsor Protocol Number: 99824 | Start Date*: 2005-03-08 | |||||||||||
Sponsor Name:Lundbeck SA | |||||||||||||
Full Title: Sertindole versus risperidone safety outcome study: A randomised, partially-blinded, parallel-group, active-controlled, post-marketing study | |||||||||||||
Medical condition: Schizophrenic patients most recently treated with antipsychotics other than sertindole or risperidone, requiring a new prescription for an antipsychotic, and without any contraindications for eithe... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006253-60 | Sponsor Protocol Number: EC07/90847 | Start Date*: 2008-04-11 | ||||||||||||||||||||||||||
Sponsor Name:MAR ESPINO HERNANDEZ | ||||||||||||||||||||||||||||
Full Title: Eficacia de la profilaxis antibiótica en dosis única nocturna frente al control clínico y tratamiento precoz de las infecciones urinarias para prevenir secuelas parenquimatosas y pielonefritis de r... | ||||||||||||||||||||||||||||
Medical condition: Demostrar que en los reflujos de alto grado (de III a V de la Clasificación Internacional del Reflujo) no hay menos incidencia de cicatrices renales ni de pielonefritis con el uso de la dosis única... | ||||||||||||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003070-26 | Sponsor Protocol Number: BLO K026 (D-CAN-546) | Start Date*: 2008-08-13 | ||||||||||||||||
Sponsor Name:Takeda Pharma GmbH | ||||||||||||||||||
Full Title: Candesartan “added” therapy for treatment optimization of symptomatic heart failure with diastolic dysfunction in diabetic and hypertensive patients. A randomized, placebo-controlled, double-blind,... | ||||||||||||||||||
Medical condition: Symptomatic heart failure with diastolic dysfunction in diabetic and hypertensive patients | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005742-39 | Sponsor Protocol Number: ARD-0301-008 | Start Date*: 2006-02-01 |
Sponsor Name:Ardana Bioscience Ltd | ||
Full Title: A Phase II single centre, open-label study investigating the pharmacokinetics, pharmacodynamics, efficacy and safety of a loading dose regimen of a new GnRH antagonist, Teverelix, long-acting formu... | ||
Medical condition: ADVANCED PROSTATE CANCER | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: LT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004201-26 | Sponsor Protocol Number: NC200602 | Start Date*: 2007-03-15 |
Sponsor Name:Neuro-Consil GmbH | ||
Full Title: Efficacy and tolerability of flexible dose adjusted pregabalin as first-line add-on treatment of patients with focal seizures | ||
Medical condition: epilepsis with seizures of focal origin | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002076-14 | Sponsor Protocol Number: EPICSstudy | Start Date*: 2014-05-12 |
Sponsor Name: | ||
Full Title: Pre-operative treatment with Erythropoietin and iron supplement for prevention of perioperative blood transfusion in cardiac surgery | ||
Medical condition: Patients (male and female) scheduled for coronary artery bypass grafting surgery (CABG) or single Aortic Valve replacement (AVR) on conventional cardiopulmonary bypass. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003685-40 | Sponsor Protocol Number: FPT1530EA | Start Date*: 2012-10-24 | |||||||||||
Sponsor Name:Thoraxkirurgisk afd. Rigshospitalet | |||||||||||||
Full Title: "Doubble blinded RCT comparing 15 versus 30mg Toradol on postoperative VAS-score in ortopedic and ENT patients. | |||||||||||||
Medical condition: Ortopedic and ENT surgery where Toradol is already given | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001332-22 | Sponsor Protocol Number: RG_12-201 | Start Date*: 2013-06-20 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: PEPtalk 2: Pilot of a randomised controlled trial to compare VZIG and aciclovir as post-exposure prophylaxis against chickenpox in children with cancer | |||||||||||||
Medical condition: Exposure to Varicella by children who have cancer. | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001100-10 | Sponsor Protocol Number: CQTI571A2314 | Start Date*: 2013-11-12 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: An open-label, multi-center protocol to provide QTI571 to PAH patients who participated in one of the extension studies and are judged by the investigator to benefit from continued QTI571 treatment | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002260-10 | Sponsor Protocol Number: MCL-metoprolol-IR | Start Date*: 2013-07-11 |
Sponsor Name:Medisch Centrum Leeuwarden | ||
Full Title: The effect of Roux-en-Y gastric bypass on the rate and extent of absorption of metoprolol from an immediate release tablet in female bariatric patient volunteers: a single oral dose study before an... | ||
Medical condition: Roux-en-Y gastric bypass | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-006123-37 | Sponsor Protocol Number: SI-C-019 | Start Date*: 2012-06-06 | |||||||||||
Sponsor Name:Solvotrin Innovations Ltd | |||||||||||||
Full Title: Impact of Eplerenone on Asymptomatic Left Ventricular Diastolic Dysfunction in Diabetic Patients | |||||||||||||
Medical condition: Asymptomatic left ventricular diastolic dysfunction in diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002068-25 | Sponsor Protocol Number: CSLCT-NHF-05-13 | Start Date*: 2006-05-23 |
Sponsor Name:CSL Limited | ||
Full Title: A Single Site, Open-Label Study to Evaluate the Immunogenicity and Safety of Enzira in Healthy 'Adults' aged >18 to <60 years and in Healthy 'Older Adults' aged >60 years for the 2006/2007 Northern... | ||
Medical condition: Prophylaxis of influenza | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003943-55 | Sponsor Protocol Number: MDS0706 | Start Date*: 2007-09-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: Clinical and biological effects of 5-Azacitidine five days/monthly schedule in symptomatic low-risk myelodysplastic syndromes (MDSs) | |||||||||||||
Medical condition: Adlut patients with low risk MDS (IPPS 0-1) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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