- Trials with a EudraCT protocol (8,950)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8,950 result(s) found.
Displaying page 127 of 448.
| EudraCT Number: 2014-001675-32 | Sponsor Protocol Number: ARTE | Start Date*: 2014-10-20 | |||||||||||
| Sponsor Name:IUCPQ | |||||||||||||
| Full Title: Aspirin versus Aspirin + ClopidogRel as Antithrombotic Treatment Following Transcatheter Aortic Valve Implantation with the Edwards Valve. A Randomized Study (the ARTE trial). | |||||||||||||
| Medical condition: Incidence of death, MI, ischemic stroke/Transient ischemic attack (TIA) or life threatening/major bleeding at 3-month follow-up. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-005310-35 | Sponsor Protocol Number: AD-03-013 | Start Date*: 2014-08-13 |
| Sponsor Name:Fundación para la Investigación en Enfermedades del Aparato Digestivo | ||
| Full Title: A phase IV double-blind, randomized, placebo-controlled, multi-center study with pancreatic enzyme replacement therapy (PERT) in subjects suffering from pancreatic exocrine insufficiency (PEI) afte... | ||
| Medical condition: Patients 2 weeks after discharge from the hospital after an attack of acute necrotizing pancreatitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-002044-41 | Sponsor Protocol Number: 38RC14.176 | Start Date*: 2014-08-18 |
| Sponsor Name:University Hospital of Grenoble | ||
| Full Title: | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-003610-86 | Sponsor Protocol Number: EMCD1403 | Start Date*: 2014-11-14 |
| Sponsor Name: | ||
| Full Title: A double blind randomized controlled trial comparing the efficacy of 7% lidocaine / 7% tetracaine cream versus 2,5% lidocaine / 2,5% prilocaine cream for local anaesthesia during laser treatment of... | ||
| Medical condition: Pain during laser treatment of: 1. Tattoo 2. Acne keloidalis nuchae | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-004799-50 | Sponsor Protocol Number: PNEUMOREG | Start Date*: 2015-02-13 |
| Sponsor Name:Federico Martinon Torres | ||
| Full Title: Evaluation of the immunoregulatory role of pneumococcal conjugate vaccination in pediatric patients with allergic asthma or type 1 diabetes mellitus versus pediatric population control. | ||
| Medical condition: Allergic asthma and type 1 diabetes mellitus in pediatric subjects. | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-003631-36 | Sponsor Protocol Number: RG_12-124 | Start Date*: 2015-02-10 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: CALiBRe: Assessment of the Mechanism of Action of idelalisib (CAL-101) in B-cell Receptor Pathway Inhibition in CLL | |||||||||||||
| Medical condition: Chronic lymphocytic leukaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001226-25 | Sponsor Protocol Number: HD-TNBC-TRIAL | Start Date*: 2015-04-20 | |||||||||||
| Sponsor Name:ISTITUTI OSPITALIERI DI CREMONA | |||||||||||||
| Full Title: A phase II randomized, open-label neo-adjuvant study of standard chemotherapy regimen compared to high dose chemotherapy regimen with autologous stem cell transplantation in patients with triple ne... | |||||||||||||
| Medical condition: Triple Negative Breast Cancer patients with breast tumor >2,5 cm | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-005786-23 | Sponsor Protocol Number: XCEL-SCI-01 | Start Date*: 2016-04-20 | |||||||||||
| Sponsor Name:Banc de Sang i Teixits | |||||||||||||
| Full Title: A phase I/IIa, randomized, double-blind, single-dose, placebo controlled, two-way crossover clinical trial to assess the safety and to obtain efficacy data in intrathecal administration of expanded... | |||||||||||||
| Medical condition: Chronic traumatic spinal cord injury | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004414-28 | Sponsor Protocol Number: BLASTO-01-2014 | Start Date*: 2015-06-10 |
| Sponsor Name:Hospital Universitari Mutua Terrassa | ||
| Full Title: Controlled, randomized trial, comparing the efficacy of paromomicin and cotrimoxazol versus metronidazol in the eradication of Blastocystis hominis in patients with gastrointestinal symptoms. | ||
| Medical condition: Gastrointestinal symptoms by Blastocystis hominis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002445-31 | Sponsor Protocol Number: SIMBA-16 | Start Date*: 2017-01-20 | ||||||||||||||||
| Sponsor Name:Enrique de Madaria | ||||||||||||||||||
| Full Title: SIMBA trial: Simvastatin in the Prevention of Recurrent Acute Pancreatitis, a Triple Blind Randomized Controlled Trial | ||||||||||||||||||
| Medical condition: Recurrent acute pancreatitis (RAP) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-001876-31 | Sponsor Protocol Number: SWAP | Start Date*: 2016-10-26 | |||||||||||
| Sponsor Name:King's College London [...] | |||||||||||||
| Full Title: Feasibility of the safe withdrawal of inhaled corticosteroids in patients with mild to moderate COPD prescribed outside guidelines (SWAP) | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-002836-42 | Sponsor Protocol Number: PRUEI | Start Date*: 2017-06-22 | |||||||||||||||||||||
| Sponsor Name:Asociación Instituto de Investigación Sanitaria BioCruces | |||||||||||||||||||||||
| Full Title: Phase II Pilot Study to assess security, potential feasibility and effectiveness of treatment with platelet rich plasma in vascular ulcers iwth difficult healing in lower extremities. | |||||||||||||||||||||||
| Medical condition: Ulcer that does not heal after being administered the optimal basic care after a period of six weeks. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2017-004137-91 | Sponsor Protocol Number: Gesida92016 | Start Date*: 2018-01-23 | |||||||||||
| Sponsor Name:Fundacion SEIMC-GESIDA | |||||||||||||
| Full Title: A single-arm, open-label, multicenter phase IV trial to evaluate the efficacy and safety of elvitegravir / cobicistat / emtricitabine / tenofovir alfa-namide as first-line treatment in naïve patien... | |||||||||||||
| Medical condition: AIDS | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002355-28 | Sponsor Protocol Number: PAP_RI1_2017/12 | Start Date*: 2018-07-12 |
| Sponsor Name:CHU of Pointe-A-Pitre | ||
| Full Title: Impact of high dose of cholecalciferol in critically ill septic patients with vitamin D deficiency: the CaribDean study | ||
| Medical condition: Morbi-mortality in critically ill patients is linked to vitamin D deficiency. Moreover, vitamin D deficiency has been related to inappropriate response to infection (due to vitamin D involvement in... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-003009-40 | Sponsor Protocol Number: CCR4326 | Start Date*: 2015-12-18 | |||||||||||||||||||||
| Sponsor Name:Royal Marsden NHS Foundation Trust | |||||||||||||||||||||||
| Full Title: Magnetic Resonance Tumour Regression Grade (mrTRG) as a Novel Biomarker to Stratify Management of Good And Poor Responders To Chemoradiotherapy: A Rectal Cancer Multicentre Randomised Control Trial | |||||||||||||||||||||||
| Medical condition: Rectal cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2017-004983-37 | Sponsor Protocol Number: FFIS-INM-2017-04 | Start Date*: 2018-10-16 |
| Sponsor Name:Fundación para la Formación e Investigación Sanitarias de la Región de Murcia | ||
| Full Title: Multicenter, randomized, prospective study to establish the clinical efficacy and the mechanisms of tolerance following immunosuppression withdrawal in liver transplantation | ||
| Medical condition: Hepatic transplant | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004299-24 | Sponsor Protocol Number: 1.0 | Start Date*: 2017-11-02 |
| Sponsor Name:Erasmus MC Kanker Instituut | ||
| Full Title: Adjuvant hepatic arterial infusion pump chemotherapy after resection of colorectal liver metastases in patients with a low clinical risk score - a feasibility study | ||
| Medical condition: Patients with resectable colorectal liver metastases | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-001143-12 | Sponsor Protocol Number: 11-EI-0264 | Start Date*: 2018-01-09 |
| Sponsor Name:The National Eye Institute | ||
| Full Title: A Pilot Study for the Evaluation of Minocycline as a Microglia Inhibitor in the Treatment of Central Retinal Vein Occlusions | ||
| Medical condition: Central Retinal Vein Occlusion | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-003413-10 | Sponsor Protocol Number: ACDHUVV-16 | Start Date*: 2016-12-20 |
| Sponsor Name:FIMABIS | ||
| Full Title: MicroRNAs expression analysis in patients undergoing cardiac surgery treated with halogenated anesthetics. Identification of microRNAs related to the cardioprotective effect | ||
| Medical condition: Cardiac surgery | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-002764-94 | Sponsor Protocol Number: OZBS82.17204 | Start Date*: 2019-07-29 | ||||||||||||||||
| Sponsor Name:Erasmus MC | ||||||||||||||||||
| Full Title: Adjuvant vaccination against HPV in surgical treatment of CIN lesions, a Randomised Controlled Trial | ||||||||||||||||||
| Medical condition: Human papilloma virus (HPV) causes cervical cancer. HPV vaccination is highly effective in primary prevention. There is less known about a possible secondary effect in women already infected with H... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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