- Trials with a EudraCT protocol (44,394)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,394 result(s) found.
Displaying page 120 of 2,220.
| EudraCT Number: 2012-001239-30 | Sponsor Protocol Number: CIR976101 | Start Date*: 2012-05-22 | |||||||||||
| Sponsor Name:Foundation for Liver Research | |||||||||||||
| Full Title: THE EFFECTS OF RECOMBINANT HUMAN INSULIN-LIKE GROWTH FACTOR-1 ON THE NUTRITIONAL STATUS IN PATIENTS WITH LIVER CIRRHOSIS: A PILOT-STUDY. | |||||||||||||
| Medical condition: Liver cirrhosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001132-22 | Sponsor Protocol Number: GEM-1202 | Start Date*: 2014-02-24 |
| Sponsor Name:Grupo Español Multidisciplinar de Melanoma | ||
| Full Title: A MULTICENTER, SINGLE ARM, PHASE 2 CLINICAL STUDY ON THE COMBINATION OF RADIATION THERAPY AND IPILIMUMAB, FOR THE TREATMENT OF PATIENTS WITH MELANOMA AND BRAIN METASTASES. | ||
| Medical condition: Patients with melanoma and brain metastases | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001143-31 | Sponsor Protocol Number: 37725 | Start Date*: 2013-07-08 | |||||||||||
| Sponsor Name:Bispebjerg University Hospital | |||||||||||||
| Full Title: TARGET “Targeting the small airways in asthma” Does fine particle ICS improve peripheral airway inflammation and function in patients with insufficient response to large particle ICS? | |||||||||||||
| Medical condition: Asthma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-004022-21 | Sponsor Protocol Number: CLDE225X2203 | Start Date*: 2013-05-08 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A Phase II multi-center, open label, randomized study to assess safety and efficacy of two different schedules of oral LDE225 in adult patients with relapsed/refractory or untreated elderly patient... | |||||||||||||
| Medical condition: relapsed/refractory or untreated acute leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Prematurely Ended) ES (Completed) GB (Prematurely Ended) IE (Prematurely Ended) SE (Prematurely Ended) NO (Completed) BE (Completed) DE (Completed) FR (Completed) NL (Completed) HU (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004025-24 | Sponsor Protocol Number: 4203/UoL000893 | Start Date*: 2013-05-20 | ||||||||||||||||
| Sponsor Name:University of Liverpool [...] | ||||||||||||||||||
| Full Title: A trial of de-escalation and stopping treatment in chronic myeloid leukaemia patients with excellent responses to tyrosine kinase inhibitor therapy DESTINY(De- Escalation and Stopping Treatment of... | ||||||||||||||||||
| Medical condition: Chronic myeloid leukaemia | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-005417-13 | Sponsor Protocol Number: 13-HMedIdeS-02 | Start Date*: 2014-04-24 |
| Sponsor Name:Hansa Medical AB [...] | ||
| Full Title: A PHASE II STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY OF INTRAVENOUS IDES AFTER ADMINISTRATION OF ASCENDING DOSES IN CHRONIC KIDNEY DISEASE PATIENTS | ||
| Medical condition: Chronic kidney disease (CKD) stage 5 and on waiting list for renal transplantation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-005546-11 | Sponsor Protocol Number: 191213 | Start Date*: 2014-07-11 | |||||||||||
| Sponsor Name:DEPARTMENT OF DERMATOLOGY, UNIVERSITY OF MODENA AND REGGIO EMILIA | |||||||||||||
| Full Title: Characterisation of maximum actinic keratosis (AK) lesions count during treatment (Lmax) by non-invasive study with high definition optical coherence tomography (HD-OCT) and reflectance confocal mi... | |||||||||||||
| Medical condition: actinic keratosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-005565-40 | Sponsor Protocol Number: OTP-B-Linköping | Start Date*: 2014-09-11 |
| Sponsor Name:Department of Biomedical Engineering, Linköping University | ||
| Full Title: Optical measurement with 5-ALA during surgical resection of brain tumors in children | ||
| Medical condition: Tumour border by means of fluorescenstechnique during surgical resection of brain tumours. | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-003923-39 | Sponsor Protocol Number: ANDA3 | Start Date*: 2013-06-25 | |||||||||||
| Sponsor Name:Tayside Medical Science Centre | |||||||||||||
| Full Title: Pilot study to evaluate whether treating persistent small airway dysfunction with extra-fine HFA-Beclometasone results in improved asthma control. | |||||||||||||
| Medical condition: Asthma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000324-34 | Sponsor Protocol Number: APD356-G000-401 | Start Date*: 2014-09-10 | ||||||||||||||||
| Sponsor Name:Eisai Limited | ||||||||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Effect of Long-Term Treatment with BELVIQ (lorcaserin HCl) on the Incidence of Major Adverse Cardiovascular Even... | ||||||||||||||||||
| Medical condition: Obese and overweight patients with cardiovascular (CV) disease and/or multiple CV risk factors | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-000344-25 | Sponsor Protocol Number: CDKO-125a-007 | Start Date*: 2013-04-22 |
| Sponsor Name:Nerviano Medical Sciences S.r.l. | ||
| Full Title: Phase II study of oral PHA-848125AC in patients with malignant thymoma previously treated with multiple lines of chemotherapy | ||
| Medical condition: Recurrent or metastatic, unresectable B3 thymoma or thymic carcinoma previously treated with multiple lines of chemotherapy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-004429-26 | Sponsor Protocol Number: Atu027-I-02 | Start Date*: 2013-02-25 | ||||||||||||||||
| Sponsor Name:Silence Therapeutics GmbH | ||||||||||||||||||
| Full Title: A Phase Ib/IIa study of combination therapy with Gemcitabine and Atu027 in subjects with locally advanced or metastatic pancreatic adenocarcinoma | ||||||||||||||||||
| Medical condition: Locally advanced or metastatic pancreatic adenocarcinoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-002816-19 | Sponsor Protocol Number: Frax001 | Start Date*: 2012-10-25 |
| Sponsor Name:Rijnstate Hospital | ||
| Full Title: Prospective, pharmacokinetic study for determination of the relationship between lean body weight and anti-Xa activity 4 hours after subcutaneous injection of 5700 IU nadroparin in morbidly obese p... | ||
| Medical condition: patients; perioperative in bariatric surgery | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004785-18 | Sponsor Protocol Number: PKBoxing-1 | Start Date*: 2014-11-18 |
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: PET imaging of neuroinflammatory consequences of chronic repetitive head injury in Muay Thai boxing | ||
| Medical condition: n/a | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004796-39 | Sponsor Protocol Number: PT-SM-14-OA | Start Date*: 2013-04-30 | ||||||||||||||||
| Sponsor Name:Fondazione IRCCS Policlinico San Matteo | ||||||||||||||||||
| Full Title: A Comparative Study of Oxycodone/Naloxone versus Codeine/Paracetamol in the Treatment of Moderate to Severe Chronic Knee and/or hip Pain Due to Osteoarthritis | ||||||||||||||||||
| Medical condition: Moderate to Severe Chronic Knee and/or hip Pain Due to Osteoarthritis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-004801-28 | Sponsor Protocol Number: HZC102972 | Start Date*: 2013-12-11 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: Multi-centre, randomized, double-blind, parallel-group study evaluating the effect of Fluticasone Furoate/ Vilanterol (FF/VI) Inhalation Powder once daily compared with Vilanterol (VI) Inhalation P... | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001670-34 | Sponsor Protocol Number: AZP01-CLI-002 | Start Date*: 2015-01-26 | |||||||||||||||||||||
| Sponsor Name:Alize Pharma | |||||||||||||||||||||||
| Full Title: A Phase IIa, randomized, double-blind, placebo-controlled, multi-center study to evaluate the safety, tolerability, and effects of AZP-531, an Unacylated Ghrelin analog, on food-related behavior in... | |||||||||||||||||||||||
| Medical condition: Prader-Willi Syndrome | |||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Completed) FR (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2014-002716-16 | Sponsor Protocol Number: NN1953-4163 | Start Date*: 2015-05-11 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: An 8-week randomised, double-blind, parallel, multiple dose trial comparing NNC0123-0000-0338 in a tablet formulation and insulin glargine in subjects with type 2 diabetes currently treated with or... | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000089-12 | Sponsor Protocol Number: HIP/FUSION#4 | Start Date*: 2018-04-24 | |||||||||||
| Sponsor Name:Institut for Klinisk Medicin, Aarhus Universitet | |||||||||||||
| Full Title: Effect and safety of the iliopsoas plane block in healthy volunteers | |||||||||||||
| Medical condition: No specific medical condition is investigated. The objective of the trial is to investigate a method for postoperative analgesia after elective hip surgery. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002667-15 | Sponsor Protocol Number: 05201401 | Start Date*: 2014-09-23 |
| Sponsor Name:Medizinische Universität Innsbruck, Innere Medizin VI | ||
| Full Title: Effect of Dual Bronchodilatation on Broncholysis Testing in COPD Patients | ||
| Medical condition: COPD (chronic obstructive pulmonary disease) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
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