- Trials with a EudraCT protocol (1,017)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,017 result(s) found for: Treatment and control groups.
Displaying page 1 of 51.
EudraCT Number: 2016-002072-26 | Sponsor Protocol Number: P150939 | Start Date*: 2016-08-25 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Multicenter randomized placebo controlled trial assessing the efficacy of oral adjuvant magnesium supplementation in the treatment of alcohol withdrawal syndrome. | |||||||||||||
Medical condition: Patients experiencing an alcohol withdrawal syndrome. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001867-22 | Sponsor Protocol Number: PRETIC | Start Date*: 2018-09-27 | |||||||||||
Sponsor Name:Banc de Sang i teixits | |||||||||||||
Full Title: TRANSFUSION OF RED BLOOD CELLS, TRANEXAMIC ACID AND FIBRINOGEN CONCENTRATE FOR SEVERE TRAUMA HEMORRHAGE AT PRE-HOSPITAL PHASE OF CARE. A PILOT TRIAL. | |||||||||||||
Medical condition: TREATMENT OF SEVERE TRAUMA HEMORRHAGE AT PRE-HOSPITAL PHASE OF CARE. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003339-21 | Sponsor Protocol Number: VEPLAN-2014-01 | Start Date*: 2015-06-02 |
Sponsor Name:Institut d'Investigació Sanitària Pere Virgili (IISPV) | ||
Full Title: Open, randomized, with two parallel treatment groups combined therapy with bleomycin and with bleomycin electrochemotherapy (EQ) in patients with plantar warts large clinical trial virus. Diagnosis... | ||
Medical condition: viral wart | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002668-29 | Sponsor Protocol Number: 132796 | Start Date*: 2020-06-25 |
Sponsor Name:University College London | ||
Full Title: A Randomised Controlled Trial of plasma exchange with standard of care compared to standard of care alone in the treatment of severe COVID-19 infection (COVIPLEX) | ||
Medical condition: COVID-19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2022-003106-72 | Sponsor Protocol Number: IIBSP-SUR-2022-61 | Start Date*: 2023-05-26 |
Sponsor Name:Institut de Recerca H. de la Santa Creu i Sant Pau | ||
Full Title: Single-blind randomized clinical trial in premature infants with Respiratory Distress Syndrome (RDS) amenable to treatment with exogenous surfactant identified early by pulmonary ultrasonography | ||
Medical condition: Respiratory Distress Syndrome | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000967-25 | Sponsor Protocol Number: ThoRaT | Start Date*: 2012-08-24 |
Sponsor Name: | ||
Full Title: Concomitant Radiotherapy and Erlotinib in advanced lung cancer ThoRaT-studien Thoracal Radiotherapy and Tarceva® An open randomized multicenter phase II study | ||
Medical condition: Non-small cell lung cancer, - palliative treatment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001628-45 | Sponsor Protocol Number: 2.0 | Start Date*: 2015-09-09 |
Sponsor Name:Dep. of Medical Cell Biology Uppsala University | ||
Full Title: A parallel, double-blinded, randomized, 6 months, two arms study with lifestyle intervention and exenatide 2 mg once weekly or lifestyle intervention and placebo in adolescents with obesity to expl... | ||
Medical condition: Obesity in adolescents | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002228-18 | Sponsor Protocol Number: AB-GEN-2013 | Start Date*: 2013-10-28 |
Sponsor Name:AB-BIOTICS S.A. | ||
Full Title: A randomized controlled clinical trial for assessing the effectiveness of pharmacogenetic information obtained with NEUROFARMAGEN in the treatment of patients with mental disorders | ||
Medical condition: Major depressive disorder schizophrenia Bipolar disorder obsessive-compulsive disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-005111-14 | Sponsor Protocol Number: HPE-4/LCR | Start Date*: 2019-04-25 |
Sponsor Name:Kepler Universitätsklinikum, Medcampus III, Klinik für Interne 2 | ||
Full Title: First-line Treatment of Helicobacter pylori with the Probiotic Lactobacillus casei rhamnosus LCR35 Alone or in Combination with a Levofloxacin-based Sequential Therapy: A Randomized, Placebo-contro... | ||
Medical condition: Helicobacter pylori infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005079-21 | Sponsor Protocol Number: LOTAB_2b_HDM | Start Date*: 2018-08-23 | |||||||||||
Sponsor Name:Lofarma S.p.A. | |||||||||||||
Full Title: A Prospective, Multicenter, Double-Blind, Placebo-Controlled, Dose-Finding Phase-II Study for the Efficacy and Safety of LAIS® House Dust Mites Sublingual Tablets in Patients with Mite-Induced Alle... | |||||||||||||
Medical condition: Patients Suffering from Mite-Induced Allergic Rhino-Conjunctivitis Without or With Controlled Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007313-68 | Sponsor Protocol Number: IG0801 | Start Date*: 2009-01-07 | |||||||||||
Sponsor Name:GRIFOLS ITALIA | |||||||||||||
Full Title: A Prospective Randomized Pilot study to evaluate the effect of preoperative antithrombin supplementation on postoperative levels of antithrombin in patients undergoing cardiac surgery with cardiopu... | |||||||||||||
Medical condition: Subjects undergoing elective cardiac surgery with Cardio Pulmonar Bypass (CPB) having baseline levels of ATIII activity equal to or higher than 60% and below 100% under all circumstances. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001596-75 | Sponsor Protocol Number: CIR-DISA-2016 | Start Date*: 2016-10-27 | |||||||||||
Sponsor Name:Fundació Parc Taulí | |||||||||||||
Full Title: Multicentre controlled, randomized clinical trial to compare the efficacy and safety of ambulatory treatment of mild acute diverticulitis without antibiotics with the standard treatment with antib... | |||||||||||||
Medical condition: Mild acute diverticulitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002061-38 | Sponsor Protocol Number: S53299 | Start Date*: 2011-06-29 | ||||||||||||||||
Sponsor Name:Katholieke Universiteit Leuven | ||||||||||||||||||
Full Title: A randomised prospective trough level monitoring study with real-time therapeutic adaptations: Trough level Adapted infliXImab Treatment scheme (TAXIT). | ||||||||||||||||||
Medical condition: 2) Crohn's disease and ulcerative colitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000607-33 | Sponsor Protocol Number: 200075 | Start Date*: 2019-06-18 |
Sponsor Name:GlaxoSmithKline S.A. | ||
Full Title: A Phase II, randomized, open-label, multicentre study to assess the reactogenicity, safety and immunogenicity of GSK’s paediatric Herpes Zoster subunit candidate vaccine (PED-HZ/su) when administer... | ||
Medical condition: Herpes Zoster Renal transplant Pediatric population | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) FR (Trial now transitioned) GB (GB - no longer in EU/EEA) IT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000979-16 | Sponsor Protocol Number: ESR-17-12784 | Start Date*: 2019-08-21 |
Sponsor Name:Dr. Guillem Cuatrecasas - CPEN S.L. | ||
Full Title: Dapagliflozin effect in the reduction of different abdominal fat layers in type 2 diabetic patients. | ||
Medical condition: Abdominal fat layers in type 2 diabetic patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001958-10 | Sponsor Protocol Number: MD2018 | Start Date*: 2018-10-25 |
Sponsor Name:Abteilung für Hals-, Nasen- und Ohrenkrankheiten MUW, AKH Wien | ||
Full Title: Dexamethasone 21-dihydrogenphosphat and Triamcinolone acetonide in the treatment of Menière´s disease: a randomized, multicentric efficacy trial | ||
Medical condition: In our study we try to evaluate the effect of intratympanic Triamcinolon acetonide and Dexamethason 21-dihydrohenphosphat on vertigo control calculation, Hydrops MRI, vHIT (video head impuls test),... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2006-004586-34 | Sponsor Protocol Number: CVAA489A2404 | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A double-blind, randomized, multicenter, parallel group study to evaluate the efficacy, tolerability, and safety of treatment with the combination of valsartan/amlodipine 160/5 mg compared to amlod... | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) FR (Completed) DE (Completed) SE (Completed) GR (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014830-10 | Sponsor Protocol Number: GCPD_27july09 | Start Date*: 2009-11-04 |
Sponsor Name:Medizinische Universität Wien, Univ.Klinik Innere Medizin III, Abt.für Nephrologie u.Dialyse | ||
Full Title: Glucose Control in Pre-Diabetic Renal Transplant Patients: Efficacy and Safety of Vildagliptin and Pioglitazone | ||
Medical condition: new onset diabetes mellitus after transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001750-25 | Sponsor Protocol Number: B9R-FP-GDGI | Start Date*: 2007-03-22 | |||||||||||
Sponsor Name:LILLY FRANCE | |||||||||||||
Full Title: Efficacy and Safety of Somatropin in Combination with Leuprorelin Compared to Somatropin Alone and to an Untreated Control Group in Pubertal Children with Idiopathic Short Stature | |||||||||||||
Medical condition: Children with Idiopathic Short Stature (ISS) at puberty onset. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000819-25 | Sponsor Protocol Number: 43712 | Start Date*: 2013-10-22 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Autologous BM derived MSCs in combination with everolimus to preserve renal structure and function in renal recipients | ||
Medical condition: renal recipients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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