- Trials with a EudraCT protocol (3,960)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (58)
3,960 result(s) found for: Multicenter trial.
Displaying page 1 of 198.
EudraCT Number: 2011-001794-85 | Sponsor Protocol Number: TRACE | Start Date*: 2011-11-01 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Transarterial RAdioembolization versus ChemoEmbolization for the treatment of HCC: A multicenter randomized controlled trial | ||
Medical condition: Patients with intermediate stage hepatocellualr carcinoma. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001131-35 | Sponsor Protocol Number: 08-0106-stop | Start Date*: 2008-05-14 |
Sponsor Name:Academic Medical Center, department of Gastroenterology and hepatology | ||
Full Title: Azathioprine maintenance treatment versus Infliximab maintenance treatment in Crohn's disease patients in remission: a randomized multicenter trial | ||
Medical condition: this study is designed as a multicenter radomized trial comparing azathioprine maintenance treatment to infliximab maintenance treatment in Crohn's disease patients that are in remission for at lea... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001346-92 | Sponsor Protocol Number: Nitroglycerin2 | Start Date*: 2008-05-23 |
Sponsor Name:No sponsor | ||
Full Title: Medical treatment with nitroglycerin for management of retained placenta - a multicentre trial | ||
Medical condition: Background: retained placenta occurs in 3% of all deliveries. The results from a pilot study indicate that medical treatment with a combination of oxytocin and the utero-relaxing agent nitroglycer... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000175-86 | Sponsor Protocol Number: CN138-180 | Start Date*: 2017-04-07 |
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, | ||
Full Title: A 52-Week, Open-label, Multicenter Study of the Safety and Tolerability of Aripiprazole Flexibly Dosed in the Treatment of Children and Adolescents with Autistic Disorder | ||
Medical condition: Autistic disorder | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-004583-30 | Sponsor Protocol Number: BIA-DPT-P2-001 | Start Date*: 2012-01-16 |
Sponsor Name:BIAL Industrial Farmaceutica | ||
Full Title: A MULTICENTER, PHASE II, RANDOMISED, DOUBLE?BLIND, PLACEBO CONTROLED CLINICAL TRIAL OF THE SUBCUTANEOUS IMMUNOTHERAPY IN DIFFERENT DOSES WITH PARALLEL GROUPS IN SUBJECTS WITH ALLERGIC RHINOCONJUNCT... | ||
Medical condition: Allergic rhinoconjunctivitis with or without associated asthma. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001995-71 | Sponsor Protocol Number: PLATIG-1404 | Start Date*: 2014-07-03 |
Sponsor Name:Plazmaferezis Állomás Közhasznú Nonprofit Kft | ||
Full Title: Open label multicenter prospective trial to assess the tetanus titer in subject of regular plasmapharesis | ||
Medical condition: healthy subjects eligible for tetanus booster vaccination | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000108-13 | Sponsor Protocol Number: UKM10_0018 | Start Date*: 2012-12-27 |
Sponsor Name:Universitätsklinikum Münster | ||
Full Title: A phase II multicenter trial with Rivaroxaban in the treatment of livedoid vasculopathy assessing the pain on a visual analog scale (VAS) | ||
Medical condition: Treatment of livedoid vasculopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005919-24 | Sponsor Protocol Number: C/399/2002 | Start Date*: 2006-07-19 |
Sponsor Name:Dr. Falk Pharma Portugal | ||
Full Title: Randomized, multicenter, double blind, placebo controlled trial, for the evaluation of the efficacy and tolerability of ursodeoxycholic acid on the dissolution of cholesterol gallstones (<15mm) aft... | ||
Medical condition: Randomized multicenter double blind, placebo controlled trial, for the evaluation of the efficacy and tolerability of UDCA on the dissolution of cholesterol gallstones (<15mm) after 18 months of th... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000674-30 | Sponsor Protocol Number: 2013-000674-30 | Start Date*: 2013-07-24 |
Sponsor Name:AOU SAN LUIGI GONZAGA - SCDU ONCOLOGIA MEDICA | ||
Full Title: Multicenter clinical trial, randomized phase II "window of opportunity" which aims to test the biological activity of abiraterone acetate administered as neoadjuvant therapy in patients with prosta... | ||
Medical condition: PROSTATE CANCER PATIENTS WITH HIGH RISK | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001766-25 | Sponsor Protocol Number: CASM981CVE01 | Start Date*: 2017-09-28 |
Sponsor Name:Novartis | ||
Full Title: An open label, 52 week, multicenter study, of long term management to evaluate effectiveness, tolerability and safety of pimecrolimus cream 1% in pediatric patients with mild to moderate atopic der... | ||
Medical condition: mild to moderate atopic dermatitis | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-003409-13 | Sponsor Protocol Number: IgPro20_3006 | Start Date*: 2015-01-05 |
Sponsor Name:CSL Behring | ||
Full Title: A Multicenter Study of Long-Term Clinical Outcomes of Immune Globulin Subcutaneous (Human) (SCIG) IgPro20 in Subjects with Primary Immunodeficiency | ||
Medical condition: Primary Immune Deficiency | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2019-004704-35 | Sponsor Protocol Number: BTX1-myalgia_pain | Start Date*: 2020-05-18 |
Sponsor Name:Region Örebro | ||
Full Title: Masseter myofascial pain relief following an intra-muscular injection with botulinum toxin type A. A randomized double-blind controlled multicenter pilot study. | ||
Medical condition: Myalgia of jaw muscle | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001781-41 | Sponsor Protocol Number: NVALT1asbestosis | Start Date*: 2019-03-07 |
Sponsor Name:Nederlandse Vereniging van Artsen voor longziekten en Tuberculose | ||
Full Title: Evaluation of safety and tolerability of pirfenidone in asbestosis, a multicenter study | ||
Medical condition: asbestosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000901-35 | Sponsor Protocol Number: 2016-02 | Start Date*: 2017-07-10 |
Sponsor Name:ASISTANCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
Full Title: Riluzole for the treatment of spasticity in the traumatic chronic spinal cord injury condition: Adaptive, Multicenter, placebo-controlled, randomised, double blind trial in a Rare Disorder” RILUSCI | ||
Medical condition: the traumatic chronic spinal cord injury condition | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003539-37 | Sponsor Protocol Number: CZOL446H2202 | Start Date*: 2016-03-07 |
Sponsor Name:Novartis | ||
Full Title: An international, multicenter, randomized, open-label, parallel efficacy, and safety trial of intravenous zoledronic acid compared to intravenous pamidronate in children with severe osteogenesis im... | ||
Medical condition: Osteogenesis Imperfecta | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2017-004417-42 | Sponsor Protocol Number: MK3475-587 | Start Date*: 2018-07-26 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Multicenter, Open label, Phase III Extension Trial to Study the Long-term Safety and Efficacy in Participants with Advanced Tumors Who Are Currently on Treatment or in Follow-up in a Pembrolizuma... | |||||||||||||
Medical condition: Advanced Tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) GB (GB - no longer in EU/EEA) NO (Trial now transitioned) SE (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) HU (Trial now transitioned) DK (Trial now transitioned) PL (Trial now transitioned) IE (Trial now transitioned) PT (Trial now transitioned) FI (Trial now transitioned) LT (Trial now transitioned) GR (Completed) IT (Trial now transitioned) LV (Trial now transitioned) EE (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002641-12 | Sponsor Protocol Number: SP833 | Start Date*: 2005-01-21 |
Sponsor Name:Schwarz Biosciences GmbH | ||
Full Title: A multicenter, multinational, phase 3b, open-label extension trial to assess the safety and tolerability of long-term treatment of rotigotine patch in subjects with idiopathic Parkinson's disease | ||
Medical condition: Parkinson's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) GB (Completed) ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003601-25 | Sponsor Protocol Number: DROP-PIP | Start Date*: 2014-03-28 |
Sponsor Name:Charité Universitätsmedizin Berlin | ||
Full Title: A multicenter, Double-blind, RandOmised, two arm Parallel group trial to determine the effects of torasemide versus furosemide on one marker (PIP) of cardiac fibrosis in patient with Diastolic Hear... | ||
Medical condition: Diastolic heart failure and diabetes mellitus type II | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-001489-24 | Sponsor Protocol Number: PSt012015 | Start Date*: 2015-11-19 |
Sponsor Name:Pharma Stulln GmbH | ||
Full Title: Prospective, controlled, randomized, investigator-masked, mul-ticenter, phase III trial to demonstrate the efficacy and safety of Brimonidine UD | ||
Medical condition: open angle glaucoma, elevated intraocular pressure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
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 |
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