- Trials with a EudraCT protocol (44,349)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,349 result(s) found.
Displaying page 584 of 2,218.
EudraCT Number: 2009-013004-31 | Sponsor Protocol Number: RASA-ROPI | Start Date*: 2009-11-02 | |||||||||||
Sponsor Name:UNIVERSITA` DEGLI STUDI DI PARMA | |||||||||||||
Full Title: Early combined prolonged release ropinirole and rasagiline therapy in newly diagnosed patients with Parkinsons disease. A prospective, randomized, parallel groups, long-term follow-up study inc... | |||||||||||||
Medical condition: Patients with Parkinson`s diesease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013027-31 | Sponsor Protocol Number: TISSUCOL | Start Date*: 2009-10-26 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: Seton or glue for transfinteric anal fistulas? Prospective randomised trial | |||||||||||||
Medical condition: transfinteric anal fistulas | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023001-36 | Sponsor Protocol Number: BAY86-4875/14607 | Start Date*: 2011-04-26 | |||||||||||
Sponsor Name:Bayer Health Care AG | |||||||||||||
Full Title: Multicenter, open-label study to evaluate the safety and efficacy (by blinded reading) of contrast-enhanced magnetic resonance angiography (MRA) after a single intravenous injection of 0.1 mmol/k... | |||||||||||||
Medical condition: Subjects with known or suspected vascular disease of the supra-aortic vessels | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) SE (Completed) FR (Completed) IT (Completed) PL (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009367-64 | Sponsor Protocol Number: PRE-SCATTO | Start Date*: 2009-04-24 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: PREEMPTIVE ANALGESIA DURING A SPRING FINGER INTERVENTION UNDER LOCAL ANAESTHESIA | |||||||||||||
Medical condition: Candidates for spring finger intervention under local anesthesia | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022408-28 | Sponsor Protocol Number: AI444-031 | Start Date*: 2010-12-10 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 2B Pilot Study of Short-Term Treatment of BMS-790052 in Combination with Peg-Interferon Alfa-2a and Ribavirin in Treatment Naive Subjects with Chronic Hepatitis C Genotype 2 or 3 Infection. | |||||||||||||
Medical condition: Chronic hepatitis C | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014532-37 | Sponsor Protocol Number: JU-AMG-403-1-1 | Start Date*: 2011-01-13 |
Sponsor Name:Universitätsklinikum Schleswig-Holstein | ||
Full Title: Effekte von oraler Cortisol oder Propranolol-Gabe auf die Verarbeitung alkoholbezogener Schlüsselreize, den Schlaf und das Rückfallrisiko von alkoholabhängigen Patienten (Copro-Studie). | ||
Medical condition: alkohol dependence | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005828-14 | Sponsor Protocol Number: NEO 013 | Start Date*: 2006-02-06 | |||||||||||
Sponsor Name:Neolab Ltd | |||||||||||||
Full Title: A phase III, Randomised, Double-blind, Double-dummy, placebo controlled crossover study to compare the systemic effects of inhaled combination Fluticasone propionate 250ug and Salmeterol xinafoate ... | |||||||||||||
Medical condition: Asthma is a chronic inflammatory disorder of the airways in which many cells and cellular elements play a role. The chronic inflammation causes an associated increase in airway hyper-responsivenes... | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021465-72 | Sponsor Protocol Number: ESAMG068 | Start Date*: 2010-10-07 | |||||||||||
Sponsor Name:Dra. Mª Dolores Arenas | |||||||||||||
Full Title: Ensayo clínico unicéntrico, abierto, no controlado, para determinar la variación en la concentración plasmática de hormona paratiroidea (PTH) en las 48 horas subsiguientes a la administración de ci... | |||||||||||||
Medical condition: Hiperparatiroidismo secundario estable | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021502-38 | Sponsor Protocol Number: LO-10-02 | Start Date*: 2011-01-25 | ||||||||||||||||
Sponsor Name:Christine Fromer Stiftung | ||||||||||||||||||
Full Title: STUDIE ZUR MESSUNG DER VAGINALEN INTERLEUKINE BEI PATIENTINNEN MIT ZERVIKALEN NEOPLASIEN (CIN 1-3) ODER CHRONISCHER CANDIDIASIS VAGINALIS UNTER BEHANDLUNG MIT 4PHENYL-BUTYRATE | ||||||||||||||||||
Medical condition: Patienten mit diagnostizierter cervikaler Neoplasie (CIN1-3) oder chronisch - rezidivierender Vaginalcandidiasis | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007299-20 | Sponsor Protocol Number: EC08/00298` | Start Date*: 2009-05-21 |
Sponsor Name:Juan Pasquau Liñao | ||
Full Title: Intervención sobre los profesionales sanitarios para reducir la duración del tratamiento antibiótico en el ámbito Hospitalario | ||
Medical condition: Neumonía adquirida en la comunidad y exacerbación aguda de la bronquitis crónica | ||
Disease: | ||
Population Age: In utero, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007305-36 | Sponsor Protocol Number: GEL-TAMO/R-GemOx-08-04/v2 | Start Date*: 2009-05-25 | ||||||||||||||||
Sponsor Name:GELTAMO (Grupo Español de Linfoma y Transplante Autólogo de Médula Ósea) | ||||||||||||||||||
Full Title: Estudio fase II prospectivo, abierto, multicéntrico de Gemcitabina, Oxaliplatino y Dexametasona + Rituximab en pacientes con linfomas agresivos (difuso de céluls grandes B y del manto) en recaída o... | ||||||||||||||||||
Medical condition: Linfoma difuso de células grandes B y Linfoma del manto | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000346-36 | Sponsor Protocol Number: BPLG-004 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:BioPartners GmbH [...] | |||||||||||||
Full Title: A Phase III, Multi-centre, Randomised, Parallel Group Study of Safety and Efficacy of the LB03002 a New Sustained Release Formulation of Human Recombinant Growth Hormone as Compared to Standard Dai... | |||||||||||||
Medical condition: pre-pubertal drug naïve growth-deficient children with insufficient endogenous growth hormone secretion | |||||||||||||
|
|||||||||||||
Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) FI (Prematurely Ended) SE (Prematurely Ended) SK (Completed) HU (Completed) CZ (Prematurely Ended) IT (Completed) DE (Completed) LT (Prematurely Ended) EE (Prematurely Ended) LV (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002941-20 | Sponsor Protocol Number: GEST | Start Date*: 2007-05-28 | |||||||||||
Sponsor Name:SECONDA UNIVERSITA' DEGLI STUDI DI NAPOLI | |||||||||||||
Full Title: RANDOMIZED PHASE II STUDY OF SORAFENIB PLUS GEMCITABINE OR SORAFENIB PLUS ERLOTINIB IN ADVANCED NON SMALL CELL LUNG CANCER (NSCLC) ELDERLY OR PS 2 PATIENTS | |||||||||||||
Medical condition: ADVANCED NON SMALL CELL LUNG CANCER (NSCLC) ELDERLY OR PS 2 PATIENTS | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003839-20 | Sponsor Protocol Number: CVT5127 | Start Date*: 2009-02-24 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Open-Label, Parallel-Group, Exploratory Study to Evaluate the Efficacy and Safety of 400 µg Regadenoson Bolus for Pharmacological Stress Echocardiography | |||||||||||||
Medical condition: Suspected coronary artery disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003843-36 | Sponsor Protocol Number: H8O-US-GWCO | Start Date*: 2008-09-19 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized Trial Comparing Exenatide with Placebo in Subjects with Type 2 Diabetes on Insulin Glargine With or Without Oral Antihyperglycemic Medications | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004625-42 | Sponsor Protocol Number: KardioPII | Start Date*: 2009-01-09 |
Sponsor Name:Asklepios Kliniken Hamburg GmbH | ||
Full Title: Percutaneous Intramyocardial Cell Therapy After Acute Myocardial Infarction using Bone Marrow Mononuclear Cells | ||
Medical condition: Acute myocardial infarction (LVEF<45%) ICD10: I21.9 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-009502-79 | Sponsor Protocol Number: ipermen | Start Date*: 2009-06-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA CAREGGI | |||||||||||||
Full Title: open, non comparative, prospectic, phase IV clinical study to evaluate the activity and tolerance of Cinacalcet-HCl (drug name Mimpara) in patients affected by MEN1-associated primary hyperparathyr... | |||||||||||||
Medical condition: Primary hyperparathyroidism in patients with MEN1 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009598-90 | Sponsor Protocol Number: 91782 | Start Date*: 2010-08-20 | |||||||||||
Sponsor Name:Bayer Health Care AG (study performed by Bayer Schering Pharma AG) | |||||||||||||
Full Title: An open label, multi-center, phase 3 study with corresponding blinded image reading to determine the efficacy and safety of a single intravenous injection of 0.1 mmol/kg body weight of gadobutrol 1... | |||||||||||||
Medical condition: Patients with histologically confirmed breast cancer referred to MRM prior to surgery after XRM. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003987-23 | Sponsor Protocol Number: NVBCA07PSP201B0 | Start Date*: 2008-06-03 |
Sponsor Name:Pierre Fabre Ibérica, S.A. | ||
Full Title: Estudio en fase II de vinorelbina oral como tratamiento neoadyuvante en pacientes de más de 60 años con cáncer de mama localmente avanzado | ||
Medical condition: Tratamiento neoadyuvante en pacientes con cáncer de mama localmente avanzado | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015255-25 | Sponsor Protocol Number: 1218.63 | Start Date*: 2010-03-03 | |||||||||||
Sponsor Name:Boehringer Ingelheim bv | |||||||||||||
Full Title: A phase III randomised, double-blind, placebo-controlled, parallel group, efficacy and safety study of linagliptin (5 mg), administered orally once daily over 24 weeks in type 2 diabetic patients (... | |||||||||||||
Medical condition: Patients with type 2 diabetes. | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DK (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
