- Trials with a EudraCT protocol (20)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
20 result(s) found for: Anhedonia AND Major Depression.
Displaying page 1 of 1.
| EudraCT Number: 2019-001907-19 | Sponsor Protocol Number: PILOT-PREXOL | Start Date*: 2019-07-03 | |||||||||||
| Sponsor Name:Region Skåne | |||||||||||||
| Full Title: Pramipexole augmentation to target anhedonia in depression - a pilot study | |||||||||||||
| Medical condition: Depression | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000439-22 | Sponsor Protocol Number: 67953964MDD3001_VENTURA-1 | Start Date*: 2023-03-08 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Randomized, Double-blind, Multicenter, Parallel-Group, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Aticaprant 10 mg as Adjunctive Therapy in Adult Participants ... | |||||||||||||
| Medical condition: Major Depressive Disorder (MDD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) CZ (Completed) ES (Ongoing) HU (Completed) BE (Completed) BG (Completed) PT (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000461-41 | Sponsor Protocol Number: 67953964MDD3002 | Start Date*: 2023-02-06 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Randomized, Double-blind, Multicenter, Parallel-Group, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Aticaprant 10 mg as Adjunctive Therapy in Adult Participants ... | |||||||||||||
| Medical condition: Major Depressive Disorder (MDD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) BG (Completed) FR (Completed) SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001539-39 | Sponsor Protocol Number: NV18-04-00260 | Start Date*: 2019-06-17 |
| Sponsor Name:Národní ústav duševního zdraví | ||
| Full Title: Clinical and neurobiological predictors of response to ketamine: towards personalized treatment of depression | ||
| Medical condition: Moderate to severe depression without psychotic symptoms | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-001997-70 | Sponsor Protocol Number: EXCELLENCE/0421/0543v1 | Start Date*: 2022-11-16 | ||||||||||||||||||||||||||
| Sponsor Name:University of Cyprus | ||||||||||||||||||||||||||||
| Full Title: Efficacy of Ketamine for the Prevention of Relapse in Patients with Opioid-Use Disorders (OUD) | ||||||||||||||||||||||||||||
| Medical condition: Methadone and buprenorphine comprise a first-line, evidence-based opioid substitution treatment (OST) for OUD patients. Unfortunately, retention and adherence to OST treatment is currently a major ... | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: CY (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2007-002740-16 | Sponsor Protocol Number: ME1-1 | Start Date*: 2007-08-23 | |||||||||||
| Sponsor Name:M's Science Corporation | |||||||||||||
| Full Title: A Phase II, Multi-Centre, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Determine the Safety and Efficacy of Treatment with SA4503, 1 mg or 3 mg Once Daily for 8 Weeks, in S... | |||||||||||||
| Medical condition: Major Depressive Disorder (MDD) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) EE (Completed) LT (Completed) LV (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022841-93 | Sponsor Protocol Number: CN162-006 | Start Date*: 2011-07-08 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-blind, Active-Controlled Study of the Efficacy and Safety of Flexibly-Dosed BMS-820836 in Patients with Treatment Resistant Major Depression Revised protocol ... | |||||||||||||
| Medical condition: Subjects with Treatment Resistant Major Depression | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-004790-31 | Sponsor Protocol Number: 55308942BIP2001 | Start Date*: 2022-05-31 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Randomized, Stratified, Double-blind, Placebo-Controlled Study to Investigate the Efficacy, Safety and Tolerability of JNJ-55308942 in Bipolar Depression | |||||||||||||
| Medical condition: Bipolar Depression | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000430-42 | Sponsor Protocol Number: 67953964MDD3003_VENTURA-LT | Start Date*: 2023-06-22 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: An Open-label, Long-term, Safety and Efficacy Study of Aticaprant as Adjunctive Therapy in Adult and Elderly Participants With Major Depressive Disorder (MDD) | |||||||||||||
| Medical condition: Major Depressive Disorder (MDD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) HU (Trial now transitioned) BE (Trial now transitioned) CZ (Trial now transitioned) PL (Trial now transitioned) BG (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) SK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001023-13 | Sponsor Protocol Number: Ox_Psych_PAXD | Start Date*: 2019-11-11 | |||||||||||
| Sponsor Name:University of Oxford / Clinical Trials and Research Governance | |||||||||||||
| Full Title: PAX-D: Randomised placebo-controlled trial evaluating the efficacy and mechanism of pramipexole as add-on treatment for people with treatment resistant depression | |||||||||||||
| Medical condition: Treatment resistant depression | |||||||||||||
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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: 2019-002704-41 | Sponsor Protocol Number: 18498A | Start Date*: 2020-03-13 | |||||||||||
| Sponsor Name:H. Lundbeck A/S | |||||||||||||
| Full Title: A randomised, double-blind, parallel-group, active controlled study evaluating the efficacy of vortioxetine versus desvenlafaxine in adult patients suffering from major depressive disorder with par... | |||||||||||||
| Medical condition: Major depressive disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) EE (Completed) LV (Completed) BG (Completed) SK (Completed) BE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005206-37 | Sponsor Protocol Number: CNTO136MDD2001 | Start Date*: 2015-09-14 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
| Full Title: A Double-Blind, Placebo-Controlled, Multicenter Study of Sirukumab as Adjunctive Treatment to a MonoAminergic antidepressant in Adults with Major Depressive Disorder | |||||||||||||
| Medical condition: Depression | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005282-22 | Sponsor Protocol Number: 42847922MDD2001 | Start Date*: 2017-10-24 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled, Adaptive Dose-Finding Study to Evaluate the Efficacy and Safety of JNJ-42847922 as Adjunctive Therapy to Antidepressants... | |||||||||||||
| Medical condition: Major Depressive Disorder (MDD) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) FI (Completed) BG (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002942-35 | Sponsor Protocol Number: CTU/2017/285 | Start Date*: 2019-10-31 | ||||||||||||||||
| Sponsor Name:University College London Comprehensive Clinical Trials Unit | ||||||||||||||||||
| Full Title: A Randomised Controlled Trial of Escitalopram and Nortriptyline compared with placebo and standard psychological care for depression in Parkinson’s Disease | ||||||||||||||||||
| Medical condition: Depression in Parkinson's disease | ||||||||||||||||||
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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: 2007-006127-12 | Sponsor Protocol Number: PNB/CPS 02 2007 | Start Date*: 2008-01-22 |
| Sponsor Name:PharmaNeuroBoost N.V. (PNB) | ||
| Full Title: Pipamperone/Citalopram (PipCit) versus Citalopram in the Treatment of Major Depressive disorder (MDD) | ||
| Medical condition: Major Depressive Disorder (MDD) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-005860-69 | Sponsor Protocol Number: ODEN | Start Date*: 2021-05-10 |
| Sponsor Name:University of Gothenburg | ||
| Full Title: OSU6162 as add-on in SSRI/SNRI-resistant depression (ODEN): a double-blind, placebo-controlled evaluation of efficacy and safety. | ||
| Medical condition: Depression | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-002604-12 | Sponsor Protocol Number: PSY-NIL-0010 | Start Date*: 2022-02-09 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Unraveling the aesthetic mind in anhedonia, insights from pharmacological imaging of the human brain: A single-blind, randomized, placebo-controlled cross-over study | ||
| Medical condition: Depression | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-000695-41 | Sponsor Protocol Number: 67953964MDD2001 | Start Date*: 2019-06-27 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Phase 2a Randomized, Double-blind, Placebo-Controlled, Parallel-Group, Multi-center Study Investigating the Efficacy, Safety, Tolerability and Pharmacokinetics of JNJ-67953964 in Subjects with Ma... | |||||||||||||
| Medical condition: Major Depressive Disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003957-16 | Sponsor Protocol Number: ZonMw80-83600-98-3074 | Start Date*: 2016-08-30 |
| Sponsor Name:University Medical Centre Groningen | ||
| Full Title: A randomised controlled trial of oral S-ketamine as add-on medication for patients with treatment-resistant major depressive disorder | ||
| Medical condition: Treatment resistant major depressive disorder | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-000219-18 | Sponsor Protocol Number: PsiloRCT001 | Start Date*: 2018-04-09 | ||||||||||||||||
| Sponsor Name:Imperial College London | ||||||||||||||||||
| Full Title: Psilocybin vs. escitalopram for major depressive disorder: comparative mechanisms | ||||||||||||||||||
| Medical condition: Major Depressive Disorder | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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