- Trials with a EudraCT protocol (44,352)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,352 result(s) found.
Displaying page 1,096 of 2,218.
EudraCT Number: 2019-002480-94 | Sponsor Protocol Number: 69HCL17_0342 | Start Date*: 2021-07-21 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Assessment of cytoreductive surgery and Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in first or secondary platinum-resistant recurrent ovarian epithelial cancer. HIPOVA-01 | |||||||||||||
Medical condition: Patients with First or second recurrence of platin-resistant epithelial ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003275-19 | Sponsor Protocol Number: 402-C-322 | Start Date*: 2013-01-29 | |||||||||||
Sponsor Name:Pacira Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Assess the Efficacy and Safety of Intercostal Nerve Block with Liposome Bupivacaine in Subjects Undergo... | |||||||||||||
Medical condition: Intercostal Nerve Block for Posterolateral Thoracotomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004624-30 | Sponsor Protocol Number: TOC17_01 | Start Date*: 2018-05-16 |
Sponsor Name:Linköping University | ||
Full Title: Modulating proinflammatory processes using tocilizumab in major depressive disorder | ||
Medical condition: Major depressive disorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-016591-68 | Sponsor Protocol Number: 09.15 | Start Date*: 2009-12-22 | ||||||||||||||||
Sponsor Name:Odense University Hospital | ||||||||||||||||||
Full Title: Placebo-controlled trial investigating the effect of Vitamin K3-lotion for the treatment of cetuximab induced folliculitis | ||||||||||||||||||
Medical condition: Cancer patients experiencing folliculitis due to treatment with cetuximab | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001208-12 | Sponsor Protocol Number: 44122 | Start Date*: 2013-08-30 |
Sponsor Name:Radboud University Nijmegen Medical Centre | ||
Full Title: Switching to aflibercept in patients with neovascular AMD not responding to anti-VEGF treatment. | ||
Medical condition: Neovascular Age-related macular degeneration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002844-25 | Sponsor Protocol Number: 12.006 | Start Date*: 2012-08-13 | ||||||||||||||||
Sponsor Name:Palle Toft | ||||||||||||||||||
Full Title: The effect of Phrenic nerve blokade on acute and chronic shoulder pain in patients for lobectomy and pneumonectomy. | ||||||||||||||||||
Medical condition: Postoperative shoulder pain, after lobectomy and pneumonectomy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000978-38 | Sponsor Protocol Number: DSIT-2015-01 | Start Date*: 2016-07-06 | |||||||||||
Sponsor Name:DAIICHI SANKYO ITALIA S.P.A. | |||||||||||||
Full Title: Randomized, prospective double-blind placebo controlled study for the evaluation of the number, duration and severity of Respiratory Tract Infections in adults with risk of recurrence after standar... | |||||||||||||
Medical condition: Evaluation of clinical efficacy of Paspat 3 mg tablets in the prevention of number, duration and severity of Respiratory Tract Infections in adults with risk, defined as affected of at least 6 epis... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004557-92 | Sponsor Protocol Number: H-19052662 | Start Date*: 2020-01-21 | |||||||||||
Sponsor Name:Steno Diabetes Center Copenhagen | |||||||||||||
Full Title: Acute effects of Sodium-glucose coTRansporter-2 inhibition on renal OxygeNation and AUTonomic function in type 1 diabetes | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000536-10 | Sponsor Protocol Number: LL-37002 | Start Date*: 2018-08-13 | |||||||||||
Sponsor Name:Promore Pharma AB | |||||||||||||
Full Title: A Study in Patients with Hard-to-Heal Venous Leg Ulcers to Measure Efficacy and Safety of Locally Administered LL-37; A Phase IIb, Double-blind, Randomised, Placebo-controlled, Multi-centre Trial | |||||||||||||
Medical condition: Hard-to-Heal (HTH) venous leg ulcer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002136-16 | Sponsor Protocol Number: RLM-MD-01 | Start Date*: 2019-04-02 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A 12-week, Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Safety and Efficacy of Relamorelin in Patients with Diabetic Gastroparesis | |||||||||||||
Medical condition: Diabetic Gastroparesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) BG (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000717-37 | Sponsor Protocol Number: AMGEVITA-HVM2019 | Start Date*: 2019-06-27 |
Sponsor Name:Fundación Publica Andaluza para la Gestión de Salud en Sevilla (FISEVI) | ||
Full Title: LOSS OF RESPONSE OF THE ADALIMUMAB BIOSIMILAR COMPARED WITH THE LOSS OF RESPONSE OF THE ADALIMUMAB ORIGINAL: CONTROLLED, RANDOMIZED, NON-INFERIORITY OPEN STUDY. "ADA-SWITCH Study" | ||
Medical condition: Inflammatory Bowel Disease: Crohn's Disease and Ulcerative Colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004195-20 | Sponsor Protocol Number: 05-7-012 | Start Date*: 2005-12-12 | |||||||||||
Sponsor Name:Astellas Pharma US, Inc. | |||||||||||||
Full Title: A Phase 3, Multi-Center, Open Label Safety Study of RSD1235 in Subjects with Atrial Fibrillation. | |||||||||||||
Medical condition: Arrhythmias are abnormal rhythms of the heart. The term arrhythmia refers to a deviation from the normal sequence of initiation and conduction of electrical impulses, which cause the heart to beat... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003233-41 | Sponsor Protocol Number: SVCARB00105 | Start Date*: 2005-10-25 | |||||||||||
Sponsor Name:Genzyme Europe BV | |||||||||||||
Full Title: An open label, dose titration study of sevelamer carbonate tablets dosed three times a day in hyperphosphatemic chronic kidney disease patients not on dialysis | |||||||||||||
Medical condition: Chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002380-24 | Sponsor Protocol Number: TC-021-IM | Start Date*: 2005-12-29 | |||||||||||
Sponsor Name:Nycomed Danmark ApS, International Medical Affairs | |||||||||||||
Full Title: An open randomised, prospective, multi-centre, parallel-group trial to compare efficacy and safety of TachoSil versus standard surgical treatment in patients undergoing pulmonary lobectomy for lung... | |||||||||||||
Medical condition: Management of pulmonary air leakage following lobectomy in subjects with lung malignancies including metastases. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) HU (Completed) DE (Completed) DK (Completed) SE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003367-23 | Sponsor Protocol Number: 672-CL-035 | Start Date*: 2006-02-13 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study of YM672 in the Treatment of Painful Bladder Syndrome/Interstitial Cystitis | |||||||||||||
Medical condition: Interstitial Cystitis / Painful Bladder Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004713-15 | Sponsor Protocol Number: 1235-SR-1005 | Start Date*: 2006-02-02 |
Sponsor Name:Cardiome Pharma Corp. | ||
Full Title: A Pilot Phase II, Randomised, Double-blind, Placebo-controlled, Multi-centred Safety, Tolerability and Preliminary Efficacy Study of RSD1235-SR for the Prevention of Atrial Fibrillation/Atrial Flut... | ||
Medical condition: Atrial fibrillation is the most common arrhythmia encountered in clinical practice. Atrial fibrillation is usually associated with age and general physical condition, rather than with a specific ca... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) CZ (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005375-16 | Sponsor Protocol Number: A-99-52120-162 | Start Date*: 2012-02-20 | |||||||||||
Sponsor Name:Institut Produits Synthèse (IPSEN) AB | |||||||||||||
Full Title: A PHASE III PROSPECTIVE, MULTI-CENTER, RANDOMISED, EVALUATOR-BLINDED STUDY TO COMPARE NEUROMUSCULAR JUNCTION (NMJ) TARGETED TECHNIQUE FOR DYSPORT INJECTIONS IN UPPER LIMB SPASTICITY POST STROKE OR ... | |||||||||||||
Medical condition: Upper limb spasticity post stroke or traumatic brain injury. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) FI (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008435-29 | Sponsor Protocol Number: 3082B2-4433-WW | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals Inc. Acting through its division Wyeth Research, a Pfizer Company | |||||||||||||
Full Title: A Non-Randomized, Open-Label Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of ReFacto AF in Previously Treated Pediatric Subjects Less Than Twelve Years of Age With Severe Hemophilia... | |||||||||||||
Medical condition: Severe hemophilia A (FVIII:C <1%) in male subjects <12 years of age. | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) IT (Completed) GR (Completed) CZ (Completed) SE (Completed) DK (Completed) FI (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000294-39 | Sponsor Protocol Number: INCB18424-363 | Start Date*: 2014-07-16 | ||||||||||||||||||||||||||
Sponsor Name:Incyte Corporation | ||||||||||||||||||||||||||||
Full Title: A Randomized, Double-Blind, Phase 3 Study of the JAK1/2 Inhibitor Ruxolitinib or Placebo in Combination With Capecitabine in Subjects With Advanced or Metastatic Adenocarcinoma of the Pancreas Who ... | ||||||||||||||||||||||||||||
Medical condition: Advanced or metastatic adenocarcinoma of the pancreas in patients that have failed or are intolerant to first-line chemotherapy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Completed) AT (Prematurely Ended) DK (Completed) PT (Prematurely Ended) NL (Prematurely Ended) FR (Prematurely Ended) IE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005231-40 | Sponsor Protocol Number: LEDA | Start Date*: 2017-03-21 | |||||||||||
Sponsor Name:UMBERTO I - POLICLINICO DI ROMA | |||||||||||||
Full Title: Effect of Aspirin on renal disease progression in patients with type 2 diabetes: a multicentre double-blind, placebo-controlled, randomised trial. The LEDA (renaL disEase progression by aspirin in ... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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