- Trials with a EudraCT protocol (56)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
56 result(s) found for: PHQ-9.
Displaying page 1 of 3.
EudraCT Number: 2009-010188-18 | Sponsor Protocol Number: 26859 | Start Date*: 2010-07-01 |
Sponsor Name:Eli Lilly Nederland | ||
Full Title: Effectiveness of Transmural Collaborative care and Duloxetine for major depressive disorder and (sub)chronic pain: a randomized placebo-controlled Multi-Centre trial. | ||
Medical condition: Major depressive disorder (episode or recurrent), as principal DSM-IV diagnosis combined with (sub)chronic pain symptoms as defined bij score of >3 on BPI painlist for at least six weeks. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004527-32 | Sponsor Protocol Number: SITADS | Start Date*: 2016-11-22 | ||||||||||||||||
Sponsor Name:King's College London [...] | ||||||||||||||||||
Full Title: Pilot randomised controlled trial of SITAgliptin for Depressive Symptoms in type 2 diabetes | ||||||||||||||||||
Medical condition: Depression in type 2 diabetes | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-005100-99 | Sponsor Protocol Number: TYH2018307 | Start Date*: 2018-06-14 |
Sponsor Name:Helsinki University and University Hospital | ||
Full Title: Pharmacoepidemiology and pharmacogenetics of antidepressant treatment for depressive disorders (PEGAD) | ||
Medical condition: Depression (ICD-10 F32 and F33). Clinically diagnosed depression (F32-33), with symptom severity equaling or exceeding score 10 in the Patient Health Questionnaire (PHQ-9) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
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: 2022-001777-31 | Sponsor Protocol Number: IG2021370 | Start Date*: 2023-05-08 |
Sponsor Name:Hospital de Neurorrehabilitación Institut Guttmann | ||
Full Title: Pilot study on the effect of cannabinoids THC + CBD on resistant spasticity in patients with chronic spinal cord injury. | ||
Medical condition: Pilot study on the effect of THC+CBD cannabinoids on resistant spasticity in patients with chronic spinal cord injury. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001624-17 | Sponsor Protocol Number: 210321 | Start Date*: 2021-07-21 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Safety of oral micronized progesterone versus norethisterone acetate in continuous combination with oral estrogen as menopausal hormone therapy – a double-blind randomized study- PROBES study (Prog... | ||
Medical condition: Climacteric symptoms | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002747-29 | Sponsor Protocol Number: BIA-2093-213 | Start Date*: 2019-04-24 | |||||||||||
Sponsor Name:Bial - Portela & Ca, S.A. | |||||||||||||
Full Title: Prevention of epilepsy in stroke patients at high risk of developing unprovoked seizures: anti-epileptogenic effects of eslicarbazepine acetate | |||||||||||||
Medical condition: Adult patients at high-risk to develop post-stroke epilepsy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) GB (GB - no longer in EU/EEA) PT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004077-16 | Sponsor Protocol Number: 14/0249 | Start Date*: 2014-12-03 | |||||||||||
Sponsor Name:University College London Joint Research Office | |||||||||||||
Full Title: A Phase IV randomised controlled trial of the selective serotonin reuptake inhibitor Sertraline versus Cognitive Behavioural Therapy for anxiety symptoms in people with Generalised Anxiety Disorder... | |||||||||||||
Medical condition: Generalised anxiety disorder (GAD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003365-34 | Sponsor Protocol Number: Artralgia1 | Start Date*: 2013-10-25 |
Sponsor Name:Specialisttandvårdskliniken Västmanlands sjukhus Västerås | ||
Full Title: Pain relief following an intra-articular single dose metylprednisolon vs. placebo on temporomandibular joint artralgia patientens. A randomized controlled blinded multicenter study. | ||
Medical condition: Artralgia of the jaw joint | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003503-35 | Sponsor Protocol Number: PAINTX | Start Date*: 2020-02-03 |
Sponsor Name:Region Östergötland | ||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group Study of the Effect of Botulinum Toxin A on Patients with Atypical Odontalgia/Persistent Dentoalveolar Pain. | ||
Medical condition: Atypical Odontalgia/Persistent Dentoalveolar Pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003311-19 | Sponsor Protocol Number: AIH-MAB | Start Date*: 2018-01-09 |
Sponsor Name:University Medical Centre Hamburg-Eppendorf | ||
Full Title: Phase IIa proof-of-principle study for the induction treatment of autoimmune hepatitis using infliximab AIH-MAB | ||
Medical condition: Autoimmune Hepatitis (AIH); rare inflammatory liver disease associated with elevated transaminases, elevated Immunoglobulin G, the presence of autoantibodies and interface hepatitis in liver histol... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001279-18 | Sponsor Protocol Number: NHSCHECK | Start Date*: 2021-03-09 |
Sponsor Name:King’s College London | ||
Full Title: Overall Study Name: NHS CHECK - Health & Experiences of staff working at NHS Trusts and Nightingale Hospitals. Embedded RCT Full Title: Effectiveness of a smartphone app-based intervention in impr... | ||
Medical condition: Mental Health and Wellbeing of Healthcare Staff | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2015-001306-33 | Sponsor Protocol Number: PQR309-005 | Start Date*: 2017-03-08 | |||||||||||
Sponsor Name:PIQUR Therapeutics AG | |||||||||||||
Full Title: Open-label, non-randomized, phase 2 study evaluating efficacy and safety of PQR309 in patients with relapsed or refractory primary CNS lymphoma | |||||||||||||
Medical condition: Relapsed or refractory primary CNS lymphoma (PCNSL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) BE (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002640-25 | Sponsor Protocol Number: 217-MDD-302 | Start Date*: 2019-12-09 | |||||||||||
Sponsor Name:Sage Therapeutics, Inc. | |||||||||||||
Full Title: A PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF THE EFFICACY AND SAFETY OF SAGE-217 WITH FIXED, REPEATED TREATMENT REGIMEN ON RELAPSE PREVENTION IN ADULTS WITH MAJOR DEPRESSIVE DIS... | |||||||||||||
Medical condition: MAJOR DEPRESSIVE DISORDER | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001424-34 | Sponsor Protocol Number: 217-PPD-301 | Start Date*: 2020-11-23 | |||||||||||
Sponsor Name:Sage Therapeutics, Inc. | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY EVALUATING THE EFFICACY AND SAFETY OF SAGE-217 IN THE TREATMENT OF ADULTS WITH SEVERE POSTPARTUM DEPRESSION | |||||||||||||
Medical condition: POSTPARTUM DEPRESSION | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001683-29 | Sponsor Protocol Number: 61393215MDD2001 | Start Date*: 2019-09-27 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: Double-Blind, Placebo-Controlled, Multi-Center Study Investigating the Efficacy, Safety, and Tolerability of JNJ-61393215 as Adjunctive Treatment in Adults with Major Depressive Disorder with Anxio... | |||||||||||||
Medical condition: Adjunctive Treatment in Adults with Major Depressive Disorder with Anxious Distress with Suboptimal Response to Standard Antidepressants | |||||||||||||
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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: 2011-002576-16 | Sponsor Protocol Number: GINECO-EN102b | Start Date*: 2013-06-11 |
Sponsor Name:ARCAGY | ||
Full Title: Phase 2 multicenter study to assess the safety and efficacy of BKM120 as monotherapy in the treatment of initial or recurrent metastatic endometrial cancer after first line therapy in patients who ... | ||
Medical condition: initial or recurrent metastatic endometrial cancer after first line therapy in patients who cannot undergo local surgery and/or radiotherapy. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002867-16 | Sponsor Protocol Number: 2017-42 | Start Date*: 2017-10-05 |
Sponsor Name:Assistance Pubique Hôpitaux de Marseille | ||
Full Title: Procollagen-3 driven corticosteroids for persistent Acute Respiratory Distress Syndrome | ||
Medical condition: Acute Respiratory Distress Syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001070-29 | Sponsor Protocol Number: CRF005 | Start Date*: 2023-05-26 | |||||||||||
Sponsor Name:Chelsea and Westminster NHS Foundation Trust | |||||||||||||
Full Title: Efficacy, tolerability and acceptability of the single tablet regimen (STR) Biktarvy® by trans people living with HIV (TPLWH) | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
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) |
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