- Trials with a EudraCT protocol (18)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
18 result(s) found for: Serotonin transporter.
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EudraCT Number: 2014-003280-38 | Sponsor Protocol Number: PSY-NIL-0006 | Start Date*: 2016-05-04 | |||||||||||
Sponsor Name:Medical University of Vienna | |||||||||||||
Full Title: Positron Emission Tomography assessment of Ketamine Binding of the Serotonin Transporter and its Relevance for Rapid Antidepressant Response | |||||||||||||
Medical condition: 20 patients with severe unipolar depression (structured clinical interview for DSM-IV and the 17-item Hamilton Depression Rating Scale), also 20 age and sex matched healthy controls. plus 12 HC f... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006576-38 | Sponsor Protocol Number: 11821 | Start Date*: 2007-09-04 |
Sponsor Name:Siegfried KASPER, O.Univ.Prof.Dr.Dr.h.c., Medizinische Universität Wien | ||
Full Title: Longitudinal imaging of serotonin transporter occupancy using PET and [11C]DASB in patients with major depression treated with escitalopram or citalopram | ||
Medical condition: Major depression | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000106-31 | Sponsor Protocol Number: 2958 | Start Date*: 2005-03-15 |
Sponsor Name:Royal Liverpool University Hospital Clinical Trials 4th floor Linda McCartney Centre | ||
Full Title: IMPACT OF CYP2D6, SEROTONIN TRANSPORTER, 5HT1, 5HT2 AND 5HT3 RECEPTOR AND MU RECEPTOR GENE POLYMORPHISMS ON EFFICACY AND TOXICITY OF TRAMADOL | ||
Medical condition: OSTEOPOROSIS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001217-25 | Sponsor Protocol Number: 2016-001217-25 | Start Date*: 2016-09-07 |
Sponsor Name:Uppsala University | ||
Full Title: Emotion, Serotonin and Premenstrual Dysphoric Disorder (EmSeP) | ||
Medical condition: Premenstrual Dysphoric Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016716-20 | Sponsor Protocol Number: 08/152/WRI | Start Date*: 2010-03-03 | |||||||||||||||||||||
Sponsor Name:Brighton and Sussex University Hospitals NHS Trust | |||||||||||||||||||||||
Full Title: Better targeting of antidepressants in older people: the influence of age and genetic background on serotonin signalling | |||||||||||||||||||||||
Medical condition: Depression | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000737-39 | Sponsor Protocol Number: AD04-301 | Start Date*: 2020-04-28 | |||||||||||
Sponsor Name:Adial Pharmaceuticals Inc. | |||||||||||||
Full Title: A 24-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 3 Clinical Study to Evaluate the Efficacy, Safety and Tolerability of AD04 (Ondansetron) in Adults with A... | |||||||||||||
Medical condition: Adult patients diagnosed with moderate or severe alcohol use disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) BG (Completed) PL (Completed) EE (Completed) LV (Completed) HR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023007-10 | Sponsor Protocol Number: TF2010 | Start Date*: 2011-03-22 | |||||||||||
Sponsor Name:Uppsala university | |||||||||||||
Full Title: A neuroscience perspective on anxiety proneness - Sex differences, monoaminergic pathways and treatment response | |||||||||||||
Medical condition: Men and women diagnosed with DSM-IV social phobia (social anxiety disorder) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005538-59 | Sponsor Protocol Number: 22-09-2008 | Start Date*: 2009-02-18 |
Sponsor Name:ZonMw | ||
Full Title: Impulsivity, a risk factor in relapse to substance use disorder: investigating neural substrates before and after pharmacological challenges | ||
Medical condition: Alcohol dependence Cocaine dependence | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001411-22 | Sponsor Protocol Number: ADAM SPECT 3792 | Start Date*: 2006-02-15 |
Sponsor Name:University School of Medicine Hannover (MHH), represented by the chairmanship | ||
Full Title: Serotonin-Transporter Binding in Tourette-Syndrome and Obsessive-Compulsive Disorder before and during Treatment with SRI: a I-123-ADAM-SPECT-Study | ||
Medical condition: Obsessive compulsive disorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-006609-25 | Sponsor Protocol Number: MOOD-HF | Start Date*: 2008-05-27 | |||||||||||
Sponsor Name:Julius Maximilians Universität Würzburg | |||||||||||||
Full Title: Effects of selective serotonin re-uptake inhibition on morbidity, mortality and mood in Depressed Heart Failure patients | |||||||||||||
Medical condition: To investigate the effects of selective serotonin re-uptake inhibition with the SSRI escitalopram on morbidity and mortality in depressed patients with CHF. The primary endpoint is the time to a fi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002560-34 | Sponsor Protocol Number: F1J-US-HMFR(b) | Start Date*: 2008-09-02 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Trial of the Efficacy and Safety of Duloxetine HCl in Patients with Central Neuropathic Pain Due to Multiple Sclerosis | |||||||||||||
Medical condition: Central neuropathic pain due to Multiple sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001343-55 | Sponsor Protocol Number: A6061030 | Start Date*: 2006-08-02 | |||||||||||
Sponsor Name:Pfizer, S.A. | |||||||||||||
Full Title: A PHASE 2B LONG-TERM, RANDOMIZED, OPEN-LABEL, SAFETY AND TOLERABILITY TRIAL COMPARING [S,S]-REBOXETINE (PNU-165442G) WITH ROUTINE CARE IN PATIENTS WITH POSTHERPETIC NEURALGIA (PHN). | |||||||||||||
Medical condition: Postherpetic neuralgia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Prematurely Ended) GB (Completed) LT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002857-18 | Sponsor Protocol Number: H9P-MC-LNBI | Start Date*: 2009-02-06 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind Comparison of LY2216684 and Placebo and Long Term Treatment with LY2216684 in Adult Patients with Major Depressive Disorder | |||||||||||||
Medical condition: Patients with Major Depressive Disorder, as defined by the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision® (DSM-IV-TR; APA 2004), | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004780-34 | Sponsor Protocol Number: A7571001 | Start Date*: 2006-04-18 | |||||||||||
Sponsor Name:Pfizer Ltd, Sandwich, UK | |||||||||||||
Full Title: An eight-week, double-blind, group sequential design, placebo controlled trial to evaluate the safety and efficacy of the co-administration of sertraline and elzasonan (CP-448,187) in outpatients w... | |||||||||||||
Medical condition: Major Depressive Disorder (MDD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000370-20 | Sponsor Protocol Number: 2448/2007 | Start Date*: 2008-08-05 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: Evaluation of pharmacokinetic and pharmacodynamic interactions between escitalopram and drugs used for the treatment of bipolar disorders. | |||||||||||||
Medical condition: bipolar disorders | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000482-36 | Sponsor Protocol Number: LUM001-201 | Start Date*: 2013-07-08 | |||||||||||
Sponsor Name:Lumena Pharmaceuticals, Inc. | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE LUM001, AN APICAL SODIUM-DEPENDENT BILE ACID TRANSPORTER INHIBITOR (ASBTi), IN COMBINATION WITH URSODEOXYCHOLIC ACID (UDCA)... | |||||||||||||
Medical condition: Primary biliary cirrhosis (PBC) is a chronic and slowly progressive cholestatic liver disease of autoimmune etiology characterized by injury of the intrahepatic bile ducts that may eventually lead ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001028-23 | Sponsor Protocol Number: T1010-01 | Start Date*: 2017-08-02 | ||||||||||||||||
Sponsor Name:Tools4Patient | ||||||||||||||||||
Full Title: Validation Study to Investigate the Effect of T4P1010 treatment in Patients with Osteoarthritic Pain of Knee or Hip. | ||||||||||||||||||
Medical condition: Osteoarthritic pain of knee or hip. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-014605-14 | Sponsor Protocol Number: F1J-US-HMGR(a) | Start Date*: 2010-01-08 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 4, 8-Week, Double-Blind, Randomized, Placebo-Controlled Study Evaluating the Efficacy of Duloxetine 60 mg Once Daily in Outpatients with Major Depressive Disorder and Associated Painful Phy... | |||||||||||||
Medical condition: Major depressive disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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