- Trials with a EudraCT protocol (339)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
339 result(s) found for: Self report.
Displaying page 1 of 17.
EudraCT Number: 2020-004487-25 | Sponsor Protocol Number: KETASELF-1 | Start Date*: 2021-02-08 |
Sponsor Name:Linköpings Universitet | ||
Full Title: Experiencing the self through touch - self-other-distinction in an altered state of self: An exploratory randomized placebo-controlled experimental medicine study | ||
Medical condition: Healthy volunteer. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003720-20 | Sponsor Protocol Number: WI231434 | Start Date*: 2019-10-16 |
Sponsor Name:University of Zagreb School of Medicine | ||
Full Title: Varenicline Versus Cytisine for Smoking Cessation in the Primary Care Setting in Croatia and Slovenia - a Randomized Controlled Trial | ||
Medical condition: Tobacco addiction | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004054-28 | Sponsor Protocol Number: Panorexia | Start Date*: 2020-06-23 | ||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||
Full Title: Psilocybin as a Treatment for Anorexia Nervosa: A Pilot Study | ||||||||||||||||||
Medical condition: Anorexia Nervosa | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003395-13 | Sponsor Protocol Number: KOA-21-02 | Start Date*: 2022-03-03 | |||||||||||
Sponsor Name:Bioventus LLC | |||||||||||||
Full Title: A Multiple Arm, Multicenter, Prospective, Randomized, Double-Blind, Placebo-Controlled, Parallel-Arm, Phase 2 Study of Intra-Articular Administration of an Allogeneic Human Placental Tissue Particu... | |||||||||||||
Medical condition: Osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004261-14 | Sponsor Protocol Number: 1703001 | Start Date*: 2019-02-12 |
Sponsor Name:Vestre Viken Trust | ||
Full Title: MUscle Side-Effects of atorvastatin in coronary patients (MUSE) | ||
Medical condition: Coronary heart disease patients With perceived statin Associated muscle symptoms or statin discontinuaton due to muscle symptoms | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-007645-12 | Sponsor Protocol Number: 250101 | Start Date*: 2008-07-15 |
Sponsor Name:University of York | ||
Full Title: The Randomised Evaluation of the Effectiveness and Acceptability of Computerised Therapy (REEACT) Trial | ||
Medical condition: Depression | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000047-33 | Sponsor Protocol Number: VitD-EX1.0 | Start Date*: 2014-03-20 |
Sponsor Name:VU University Medical Centre | ||
Full Title: The effect of high-resistance muscle strength training and vitamin D supplementation in persons with knee osteoarthritis | ||
Medical condition: knee osteoarthritis vitamin D deficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003137-40 | Sponsor Protocol Number: F02207GE302 | Start Date*: 2015-09-28 |
Sponsor Name:Pierre Fabre Medicament | ||
Full Title: A European Phase III, Multicentre, Double-blind, Randomised, Placebo-Controlled Monotherapy Study of Milnacipran for the Treatment of the Fibromyalgia Syndrome. | ||
Medical condition: Fibromyalgia, also known as FMS, is a common systemic rheumatologic disorder estimated to affect 2 to 4% of the population Fibromyalgia is associated with a reduced threshold for pain, generally i... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) FI (Completed) SE (Completed) ES (Completed) PT (Completed) DE (Completed) GB (Completed) CZ (Completed) IT (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001411-12 | Sponsor Protocol Number: CBYM338B2203E1 | Start Date*: 2015-11-04 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: Extension of the CBYM338B2203 phase IIb/III study to evaluate the long-term efficacy, safety and tolerability of intravenous BYM338 in patients with sporadic inclusion body myositis | |||||||||||||
Medical condition: Sporadic Inclusion Body Myositis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) NL (Completed) DK (Completed) GB (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001965-36 | Sponsor Protocol Number: FAAHIPTSD | Start Date*: 2020-08-26 |
Sponsor Name:Linkoping University | ||
Full Title: Effects of the FAAH inhibitor JNJ-42165279 in combination with internet-based cognitive behavioral therapy in PTSD | ||
Medical condition: post traumatic stress disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004984-11 | Sponsor Protocol Number: P150962J | Start Date*: 2018-07-06 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: "Study of maintenance of the efficacy and adverse effects of pharmacological treatments in sex offenders with paraphilia" ESPARA | |||||||||||||
Medical condition: Sexual offenders with paraphilia | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000324-17 | Sponsor Protocol Number: GA18/118305 | Start Date*: 2019-08-02 | ||||||||||||||||
Sponsor Name:University of Leeds | ||||||||||||||||||
Full Title: Amitriptyline at Low-dose and Titrated for Irritable Bowel Syndrome as Second-line Treatment (The ATLANTIS study): A Double-blind Placebo-controlled Trial | ||||||||||||||||||
Medical condition: Irritable Bowel Syndrome (IBS) | ||||||||||||||||||
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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: 2019-003959-11 | Sponsor Protocol Number: 1703001 | Start Date*: 2020-05-25 |
Sponsor Name:Vestre Viken Trust | ||
Full Title: MUscle Side-Effects of atorvastatin in coronary patients (MUSE) follow-up study | ||
Medical condition: Coronary heart disease patients With perceived statin Associated muscle symptoms or statin discontinuaton due to muscle symptoms | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000087-42 | Sponsor Protocol Number: TAISTR_2016 | Start Date*: 2016-05-11 |
Sponsor Name:University College Dublin | ||
Full Title: A multicentre, prospective, single arm, open-label 96 week observational trial of the tolerability, adherence and efficacy of a dolutegravir/abacavir/lamivudine single tablet regimen in HIV-1 antib... | ||
Medical condition: Human Immunodeficiency Virus (HIV) infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-005006-66 | Sponsor Protocol Number: 2013118 | Start Date*: 2014-01-21 |
Sponsor Name:Procter and Gamble | ||
Full Title: A 2-arm, randomised, single - (Investigator) blind, controlled, parallel design study in common cold sufferers experiencing nasal congestion to assess the speed of action of Vicks® VapoRub® (VVR) | ||
Medical condition: Nasal congestion due to common cold in adults | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004937-15 | Sponsor Protocol Number: BNC210.006 | Start Date*: 2015-04-16 | |||||||||||
Sponsor Name:BIONOMICS LIMITED | |||||||||||||
Full Title: A randomized, double-blinded, placebo and lorazepam-controlled, four-way crossover, Phase II study to evaluate the effects of single oral administration of BNC210 on brain activity changes captured... | |||||||||||||
Medical condition: Generalized Anxiety Disorder | |||||||||||||
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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: 2019-002813-20 | Sponsor Protocol Number: 331-201-00242 | Start Date*: 2020-03-16 | ||||||||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | ||||||||||||||||||
Full Title: A Multicenter, Randomized, Flexible-dose, Double-blind Trial of Brexpiprazole Versus Placebo for the Treatment of Adults With Borderline Personality Disorder | ||||||||||||||||||
Medical condition: Borderline Personality Disorder | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000281-23 | Sponsor Protocol Number: Oxford University(None) | Start Date*: 2009-09-10 | ||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||
Full Title: Melatonin in Acute Mania Investigation (MIAMI-UK) | ||||||||||||||||||
Medical condition: Bipolar Disorder (mania and hypomania) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000180-70 | Sponsor Protocol Number: 2020-09(04) | Start Date*: 2021-05-31 |
Sponsor Name:Beacon Hospital | ||
Full Title: Knee osteoarthritis Injection Therapy (KNiT) trial | ||
Medical condition: Knee osteoarthritis (OA). Osteoarthritis (OA) is a debilitating disease which mostly affects people over 60 years of age. It is known to be within the top 10 contributors to years lived with disabi... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004513-33 | Sponsor Protocol Number: OCTUMI-02 | Start Date*: 2008-05-08 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: Comparative Evaluation of QUEtiapine-Lamotrigine combination versus quetiapine monotherapy (and folic acid versus placebo) in patients with bipolar depression | |||||||||||||
Medical condition: Bipolar depression | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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