- Trials with a EudraCT protocol (43)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
43 result(s) found for: Mind.
Displaying page 1 of 3.
EudraCT Number: 2015-005322-19 | Sponsor Protocol Number: MIND-DC | Start Date*: 2016-01-21 |
Sponsor Name:Radboud University Nijmegen Medical Centre | ||
Full Title: A randomized, double-blind, placebo-controlled phase III study to evaluate active immunization in adjuvant therapy of patients with stage IIIB and IIIC melanoma with natural dendritic cells pulsed ... | ||
Medical condition: melanoma patients with regional lymph node metastases (stage III) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015821-34 | Sponsor Protocol Number: 6520-9961-03 | Start Date*: 2010-07-13 |
Sponsor Name:MEDICE Arzneimittel GmbH & Co. KG | ||
Full Title: Dosisfindungsstudie zu Nicotinamid bei dialysepflichtigen Patienten mit Hyperphosphatämie | ||
Medical condition: Hyperphosphatämie bei dialysepflichtigen Patienten | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-007156-33 | Sponsor Protocol Number: CRO970 (MIND) | Start Date*: 2008-05-23 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: Melatonin As A Novel Neuroprotectant in Preterm Infants- Dosage study | |||||||||||||
Medical condition: Brain Injury in Preterm Infants | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015826-13 | Sponsor Protocol Number: Q-10 | Start Date*: 2010-10-07 | |||||||||||
Sponsor Name:PROF. TIZIANO GHERLI | |||||||||||||
Full Title: THE USE OF COENZYME Q 10 BEFORE HEART SURGERY IN ELDERLY PATIENTS. | |||||||||||||
Medical condition: Patients (male or female) aged > 70 years, clinically stable, with a diagnosis of severe aortic stenosis with indication to surgery based on echocardiography and left ventricle angiography. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002152-18 | Sponsor Protocol Number: 2004-0827 | Start Date*: 2005-08-31 |
Sponsor Name:Prof. Dr. H. Lode | ||
Full Title: Untersuchung über die Empfindlichkeitsveränderungen oraler Mundstreptokokken gegenüber Makrolidantibiotika nach Gabe von AzithromycinSR versus ClarithromycinXL bei freiwilligen gesunden Probanden | ||
Medical condition: keine Erkrankung (gesunde Probanden) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000206-36 | Sponsor Protocol Number: DOPA1 | Start Date*: 2014-10-27 |
Sponsor Name: | ||
Full Title: DRD4 genotype as a moderator of L-Dopa intervention effects on parent-related neurocognitive processes, behaviors, and attitudes: A micro-trial of differential susceptibility to pharmacological int... | ||
Medical condition: There are no medical conditions or diseases under investigation. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005927-19 | Sponsor Protocol Number: GESIDA11920 | Start Date*: 2022-05-17 | |||||||||||
Sponsor Name:Fundación SEIMC-GESIDA | |||||||||||||
Full Title: Phase IV, randomized, multicenter, double-blind clinical trial designed to evaluate the safety and convenience of switching from Dolutegravir/Lamivudine to Bictegravir/Emtricitabine/Tenofovir alafe... | |||||||||||||
Medical condition: Human immunodeficiency virus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005072-32 | Sponsor Protocol Number: R&D2004/39 | Start Date*: 2005-12-19 |
Sponsor Name:Kings College London (IOP) / South London and Maudsley NHS Trust (Co-sponsorship) | ||
Full Title: Is it possible to modify the course of manic relapse? A pilot study of the effectiveness of quetiapine in preventing the development of manic episodes in Bipolar Disorder. | ||
Medical condition: Bipolar Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001827-12 | Sponsor Protocol Number: D-IIS-BP-01 | Start Date*: 2005-12-29 |
Sponsor Name:Georg-August-Universität Göttingen, Bereich Humanmedizin | ||
Full Title: Myfortic ® zur Therapie des Bullösen Pemphigoids. Eine offene monozentrische proof-of-concept Studie | ||
Medical condition: Bullous Pemphigoid | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-003885-19 | Sponsor Protocol Number: NOT-APPLICABLE-HUFA | Start Date*: 2023-03-15 |
Sponsor Name:NO-COMERCIAL | ||
Full Title: ECOGUIDED GENICULAR NERVE BLOCK IN PATIENTS WITH KNEE OSTEOARTHRITIS BY LOCAL ANESTHETIC OR BY COMBINATION OF LOCAL ANESTHETIC AND CORTICOID: PLACEBO-CONTROLLED RANDOMIZED BLIND CLINICAL TRIAL | ||
Medical condition: KNEE OSTEOARTHRITIS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004180-43 | Sponsor Protocol Number: BAY59-7939/15786 | Start Date*: 2013-03-13 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A randomized controlled trial of rivaroxaban for the prevention of major cardiovascular events in patients with coronary or peripheral artery disease (COMPASS - Cardiovascular OutcoMes for People u... | |||||||||||||
Medical condition: Prevention of major cardiovascular events in patients with coronary or peripheral artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) SE (Completed) CZ (Completed) FI (Completed) IT (Completed) HU (Completed) NL (Completed) GB (Completed) SK (Completed) DK (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001098-55 | Sponsor Protocol Number: MMED007 | Start Date*: 2021-11-24 |
Sponsor Name:Mind Medicine, Inc. | ||
Full Title: Safety and efficacy of repeated low dose D-lysergic acid diethylamide (LSD) D-Tartrate (MM-120) as treatment for ADHD in adults: a multi-center, randomized, double- blind, placebo-controlled Phase ... | ||
Medical condition: Attention-Deficit/Hyperactivity Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003466-33 | Sponsor Protocol Number: 1103-011 | Start Date*: 2013-05-17 | |||||||||||
Sponsor Name:Mental Health Services North Holland North | |||||||||||||
Full Title: Memantine Add-On Therapy to Clozapine | |||||||||||||
Medical condition: Cognitive functioning, severity of psychopathology and treatment response (positive symptoms and negative symptoms of schizophrenia), depressive symptoms, social cognition, obsessive-compulsive sy... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004419-24 | Sponsor Protocol Number: RHMMED0687 | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:Southampton University Hospitals Trust (R&D) | |||||||||||||
Full Title: The Use of Sulfasalazine as an Anti-fibrotic in Acute Alcoholic Hepatitis | |||||||||||||
Medical condition: Acute Alcoholic Hepatitis | |||||||||||||
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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: 2012-004504-35 | Sponsor Protocol Number: RF-2010-2311148 | Start Date*: 2013-02-26 | |||||||||||
Sponsor Name:IRCCS CENTRO SAN GIOVANNI DI DIO FATEBENEFRATELLI | |||||||||||||
Full Title: The use of Oxytocin as adjunctive therapy for the treatment of schizophrenia: a randomized, double blind trial | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011856-23 | Sponsor Protocol Number: ERNPL | Start Date*: 2009-09-16 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: Evaluation of acute postsurgery pain management in patients who undergo inguen hernia surgery | |||||||||||||
Medical condition: Acute post surgery pain in patients who undergo inguen hernia surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002446-31 | Sponsor Protocol Number: FMLD-HUNGRIA-28_FIII | Start Date*: 2017-03-08 |
Sponsor Name:LABORATORIOS FARMALIDER S.A. | ||
Full Title: Phase III clinical trial , multicenter , randomized , double-blind , crossover, active-controlled and placebo to evaluate the analgesic efficacy and safety of paracetamol / ibuprofen 500/200 mg com... | ||
Medical condition: MODERATE TO SEVERE PAIN FOLLOWING DYSMENORRHOEA | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005452-26 | Sponsor Protocol Number: SMR-2728 | Start Date*: 2015-11-19 | |||||||||||
Sponsor Name:OptiNose AS | |||||||||||||
Full Title: A randomized, placebo controlled, double-blind, double-dummy, 3-period cross-over study in adult patients with autism spectrum disorders evaluating cognitive response, eye-gaze, and heart rate vari... | |||||||||||||
Medical condition: Autism spectrum disorder | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021901-19 | Sponsor Protocol Number: PHANOS | Start Date*: 2011-05-05 | |||||||||||
Sponsor Name:Med Uni Graz, Univ. Klinik für Anästhesiologie und Intensivmedizin | |||||||||||||
Full Title: Reduzierter Opioidverbrauch durch Physostigmin als Dauertropf zur postoperativen PCA – PHANOS (PHysostigmine-enhANced Opioid analgeSia). prospektive, doppelblinde, randomisierte, placebokontrollie... | |||||||||||||
Medical condition: Die Hypothese dieser prospektiven, doppelblinden, randomisierten, placebokontrollierten Studie ist, dass die kontinuierliche i.v. Gabe von Physostigmin während der ersten 24 h postoperativ zu einem... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004226-82 | Sponsor Protocol Number: 10077 | Start Date*: 2006-09-07 | |||||||||||
Sponsor Name:University Hospitals of Leicester NHS Trust | |||||||||||||
Full Title: PHARMACODYNAMIC STUDY OF ORAL MIRTOSELECT IN PATIENTS WITH SUSPECTED COLORECTAL DISEASE | |||||||||||||
Medical condition: Patients with operable colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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