- Trials with a EudraCT protocol (44,380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,380 result(s) found.
Displaying page 820 of 2,219.
| EudraCT Number: 2017-000613-22 | Sponsor Protocol Number: CO-150225133959-HRCT | Start Date*: 2018-10-15 |
| Sponsor Name:Johnson & Johnson Consumer Inc | ||
| Full Title: A 16 Week, Single-center, Randomized, Placebo- and Active-controlled Proof of Principle Study to Assess the Efficacy and Safety of a 5% Minoxidil Topical Gel Formulation in Male subjects with Andro... | ||
| Medical condition: Alopecia Androgentica | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001756-35 | Sponsor Protocol Number: 16/0163 | Start Date*: 2019-06-21 | |||||||||||
| Sponsor Name:University of California, San Francisco | |||||||||||||
| Full Title: A Randomized, Double-Blind, Parallel-Group, Placebo Controlled Trial to Assess the Efficacy, Safety, Tolerability, and Pharmacokinetics of Clemastine Fumarate as a Remyelinating Agent in Acute Opti... | |||||||||||||
| Medical condition: acute optic neuritis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003406-11 | Sponsor Protocol Number: NN1436-4465 | Start Date*: 2019-04-09 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: A trial comparing NNC0148-0287 C (insulin 287) versus insulin glargine U100, both in combination with metformin, with or without DPP4 inhibitors and with or without SGLT2 inhibitors, in insulin-naï... | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SK (Completed) PL (Completed) HU (Completed) ES (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004741-27 | Sponsor Protocol Number: DM14/11351 | Start Date*: 2015-02-18 | |||||||||||
| Sponsor Name:University of Leeds | |||||||||||||
| Full Title: Comparison of Alitretinoin with PUVA as the first line treatment in patients with severe chronic hand eczema | |||||||||||||
| Medical condition: Severe chronic hand eczema | |||||||||||||
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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: 2014-001513-35 | Sponsor Protocol Number: | Start Date*: 2016-08-23 | ||||||||||||||||
| Sponsor Name:NHS Blood and Transplant. [...] | ||||||||||||||||||
| Full Title: TREATT: TRial to EvaluAte Tranexamic acid therapy in Thrombocytopenia A double blind, randomised controlled trial evaluating the safety and efficacy of Tranexamic acid in patients with haematologic... | ||||||||||||||||||
| Medical condition: Bleeding secondary to thrombocytopaenia associated to haematological malignancies. | ||||||||||||||||||
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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: 2017-002225-38 | Sponsor Protocol Number: 331-201-00083 | Start Date*: 2018-02-23 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
| Full Title: A Multicenter, Open-label Trial to Evaluate the Safety and Tolerability of Brexpiprazole in the Treatment of Subjects with Bipolar I Disorder | |||||||||||||
| Medical condition: Treatment of Manic Episodes Associated with Bipolar I Disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) PL (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003284-62 | Sponsor Protocol Number: 012508 | Start Date*: 2019-07-18 |
| Sponsor Name:Queen Mary University London | ||
| Full Title: A randomised, blinded, placebo controlled, Phase 2a study to evaluate the safety and efficacy of administering Regadenoson to patients with critical injury and signs of haemorrhagic shock | ||
| Medical condition: Cardiovascular collapse following traumatic haemorrhage | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004729-34 | Sponsor Protocol Number: NOV-FR04 | Start Date*: 2019-05-21 |
| Sponsor Name:Medical Center- Universtíty of Freiburg Department of Child and Adolescent Psychiatry, Psychotherapy and Psychosomatics | ||
| Full Title: Effects of transdermal estrogen on Bone Mass in adolescent female patients with Anorexia nervosa (AN) – a placebo-controlled, double-blind, randomized, interventional study | ||
| Medical condition: Anorexia nervosa | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002784-18 | Sponsor Protocol Number: 13005 | Start Date*: 2018-07-24 | |||||||||||
| Sponsor Name:Clinical Trials and Research Governance | |||||||||||||
| Full Title: Safety and efficacy of Tofacitinib in ameliorating ischaemia reperfusion injury and allograft pancreatitis in solid organ transplantation – a pilot study | |||||||||||||
| Medical condition: Ischaemia reperfusion injury and allograft pancreatitis. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-002284-10 | Sponsor Protocol Number: INS-4582 | Start Date*: 2019-06-25 | |||||||||||||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||||||||||||
| Full Title: A TRIAL TO COMPARE THE INJECTION SITE EXPERIENCE OF 0.25 MG SEMAGLUTIDE SC ADMINISTERED BY 2 DIFFERENT PRODUCTS | |||||||||||||||||||||||
| Medical condition: Healthy volunteers (Diabetes Mellitus, Type 2) (Overweight) (Obesity) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2017-004645-24 | Sponsor Protocol Number: 206852 | Start Date*: 2018-11-09 | |||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | |||||||||||||
| Full Title: A randomized, double blind, controlled mechanistic study of rituximab and belimumab combination therapy in PR3 ANCA-associated vasculitis | |||||||||||||
| Medical condition: ANCA-associated vasculitis | |||||||||||||
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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: 2018-000992-34 | Sponsor Protocol Number: 17915A | Start Date*: 2018-11-13 | |||||||||||
| Sponsor Name:H. Lundbeck A/S | |||||||||||||
| Full Title: Interventional, randomized, double-blind, placebo-controlled study of the efficacy and safety of initial administration of 25 mg vortioxetine intravenously with 10 mg/day vortioxetine orally in ... | |||||||||||||
| Medical condition: Major Depressive disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) EE (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-000205-77 | Sponsor Protocol Number: KF5503-75 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Grünenthal GmbH | |||||||||||||
| Full Title: Open-label investigation of the pharmacokinetic profile, safety, tolerability, and efficacy of multiple administrations of tapentadol oral solution used for treatment of acute pain in children aged... | |||||||||||||
| Medical condition: Moderate to severe acute pain | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004986-15 | Sponsor Protocol Number: Protocol_AFCN_17022019 | Start Date*: 2019-02-18 | |||||||||||||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
| Full Title: Ultrasound-guided nerve block of the anterior femoral cutaneous nerves in healthy volunteers | |||||||||||||||||||||||
| Medical condition: Pain around the surgical incision after total knee arthroplasty (TKA). The area anesthetized by a combination of nerve block techniques anesthetizing the anterior femoral cutaneous nerves are inve... | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2015-000641-23 | Sponsor Protocol Number: CNWL/MC/AFT/01 | Start Date*: 2015-11-24 |
| Sponsor Name:Central and North West London NHS Foundation Trust | ||
| Full Title: Aggression Following TBI: Effectiveness of Risperidone (AFTER)-a feasibility RCT. | ||
| Medical condition: aggression and agitation following on from a traumatic brain injury | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-003113-17 | Sponsor Protocol Number: MEU17/361 | Start Date*: 2018-11-09 | |||||||||||
| Sponsor Name:The Medicines Evaluation Unit (MEU) Ltd. (Investigator led study) | |||||||||||||
| Full Title: A randomised, open label 2-way cross-over study to compare the effects of inhaled Beclometasone/Formoterol/Glycopyrronium (TRIMBOW) pMDI to Beclometasone/Formoterol (FOSTAIR) pMDI on hyperinflation... | |||||||||||||
| Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001237-14 | Sponsor Protocol Number: LIGRADIS | Start Date*: 2019-06-11 | |||||||||||
| Sponsor Name:Dr. Jesús María Villar del Moral and Dr. José Luis Muñoz de Nova | |||||||||||||
| Full Title: Randomized clinical trial, blinded for the researcher and multicenter, to evaluate the efficacy and safety of preoperative preparation with Lugol solution in euthyroid patients with Graves-Basedow ... | |||||||||||||
| Medical condition: Graves-Basedow disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001656-19 | Sponsor Protocol Number: RP-L301-0119 | Start Date*: 2019-09-19 | |||||||||||
| Sponsor Name:Rocket Pharmaceuticals, Inc. | |||||||||||||
| Full Title: Gene Therapy for Pyruvate Kinase Deficiency (PKD): A Phase I Clinical Trial to Evaluate the Safety of the Infusion of Autologous CD34+ Cells Transduced with a Lentiviral Vector Carrying the Codon O... | |||||||||||||
| Medical condition: Pyruvate kinase deficiency | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001305-82 | Sponsor Protocol Number: IC3627/18 | Start Date*: 2019-05-16 |
| Sponsor Name:Laura Perelló Moreno | ||
| Full Title: Study on the advantages of local post-operative infiltration in forefoot surgery. | ||
| Medical condition: management of postoperative pain in ambulatory foot surgery that allows the realization of immediate rehabilitation and better functional results and personal satisfaction | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-003936-62 | Sponsor Protocol Number: PRONE | Start Date*: 2019-06-13 | ||||||||||||||||
| Sponsor Name:HOSPITAL UNIVERSITARI DE BELLVITGE-IDIBELL | ||||||||||||||||||
| Full Title: RENINE ANGIOTENSINE SYSTEM BLOCKADE (RAAS) IN RENAL TRANSPLANT RECIPIENTS WITH RENAL PROGENITOR CELLS (PEC's) IN URINE: RANDOMIZED CLINICAL TRIAL | ||||||||||||||||||
| Medical condition: POST TRANSPLANT RENAL GLOMERULOPATHY | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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