- Trials with a EudraCT protocol (600)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
600 result(s) found for: Severity of illness.
Displaying page 1 of 30.
EudraCT Number: 2018-001615-78 | Sponsor Protocol Number: F1J-MC-HMGW | Start Date*: 2018-05-02 |
Sponsor Name: | ||
Full Title: Effect of Duloxetine 30/60 mg Once Daily Versus Placebo in Adolescents With Juvenile Primary Fibromyalgia Syndrome | ||
Medical condition: Juvenile Primary Fibromyalgia Syndrome | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-004471-23 | Sponsor Protocol Number: CB/ALICE/0010 | Start Date*: 2015-08-12 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: Antivirals for influenza Like Illness? An rCt of Clinical and Cost effectiveness in primary CarE | |||||||||||||
Medical condition: Influenza-like illness | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) IE (Completed) GB (Completed) SE (Completed) CZ (Completed) LT (Completed) DK (Completed) NL (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001006-41 | Sponsor Protocol Number: ETHIC_pilot | Start Date*: 2018-09-03 |
Sponsor Name:Academisch Medisch Centrum | ||
Full Title: The Efficacy of TRH in Intensive Care patients; a dose finding study | ||
Medical condition: Non thyroidal illness syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001103-77 | Sponsor Protocol Number: FLU007INVICTUS | Start Date*: 2017-09-05 | ||||||||||||||||
Sponsor Name:Vaccitech Limited | ||||||||||||||||||
Full Title: A phase IIb study to determine the safety and efficacy of candidate INfluenza Vaccine MVA-NP+M1 in combination with licensed InaCTivated inflUenza vaccine in adultS aged 65 years and above | ||||||||||||||||||
Medical condition: Influenza | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002503-19 | Sponsor Protocol Number: 62586 | Start Date*: 2020-07-08 | |||||||||||
Sponsor Name:UMC Utrecht | |||||||||||||
Full Title: BCG vaccination to Reduce the impact of COVID-19 in healthcare workers (BRACE) Trial | |||||||||||||
Medical condition: SARS-CoV-2 infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003904-15 | Sponsor Protocol Number: 20202407 | Start Date*: 2020-08-27 | |||||||||||
Sponsor Name:University of Southern Denmark | |||||||||||||
Full Title: Using BCG vaccine to enhance non-specific protection of senior citizens during the COVID-19 pandemic. A randomized clinical trial. | |||||||||||||
Medical condition: Healthy volunteers, senior citizens of 65 years or older. Immune system activation after BCG vaccination. Acute infections, COVID-19 and self-reported respiratory illness will be monitored. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000160-42 | Sponsor Protocol Number: M2016 | Start Date*: 2016-05-17 | |||||||||||
Sponsor Name:UK für Anästhesiologie und allgemeine Intensivmedizin | |||||||||||||
Full Title: Effect of inhaled budenoside on the incidence and severity of Acute Mountain Sickness at 4559 m | |||||||||||||
Medical condition: Healthy volunteer trial at 4459m to investigate the effect of inhaled budenoside on the incidence and severity of Acute Mountain Sickness. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004042-26 | Sponsor Protocol Number: PrEP-CS-002 | Start Date*: 2015-11-17 | |||||||||||
Sponsor Name:hVIVO Services Limited | |||||||||||||
Full Title: A Phase II, Double-Blinded, Randomised, Controlled Study to Examine the Prophylactic Efficacy, Safety and Tolerability of PrEP-001 in Asthmatic Subjects Subsequently Challenged with Human Rhinoviru... | |||||||||||||
Medical condition: Human Rhinovirus (HRV-16) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004872-31 | Sponsor Protocol Number: SCA102833 | Start Date*: 2016-12-21 | |||||||||||
Sponsor Name:GlaxoSmithKline | |||||||||||||
Full Title: The Evaluation of Lamictal as an Add-on Treatment for Bipolar I Disorder in Children and Adolescents, 10 to 17 Years of Age | |||||||||||||
Medical condition: Bipolar Disorder | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000757-13 | Sponsor Protocol Number: RGH-MD-54 | Start Date*: 2016-06-07 | |||||||||||
Sponsor Name:Forest Laboratories LLC, an Allergan Affiliate | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter, Fixed-Dose Clinical Trial Evaluating the Efficacy, Safety and Tolerability of Cariprazine in Patients with Bipo... | |||||||||||||
Medical condition: Bipolar I Depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LT (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002055-15 | Sponsor Protocol Number: J81J1100168007 | Start Date*: 2014-01-28 |
Sponsor Name:UNIVERSITY OF SASSARI | ||
Full Title: RANDOMIZED, CONTROLLED, MULTI-CENTER, INTERNATIONAL CLINICAL STUDY ON THE MOOD-STABILIZING EFFECTS OF MEMANTINE AS AN AUGMENTING AGENT vs. LAMOTRIGINE FOR ONGOING TREATMENT IN BIPOLAR-I DISORDER P... | ||
Medical condition: BIPOLAR I MOOD DISORDERS | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003268-25 | Sponsor Protocol Number: AT-03A-017 | Start Date*: 2023-05-12 | |||||||||||
Sponsor Name:Atea Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Bemnifosbuvir in High-Risk Outpatients with COVID-19 | |||||||||||||
Medical condition: COVID-19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) ES (Ongoing) LV (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000468-27 | Sponsor Protocol Number: BVX-010 | Start Date*: 2018-07-04 | |||||||||||
Sponsor Name:BiondVax Pharmaceuticals Ltd. | |||||||||||||
Full Title: A pivotal, multicentre, randomized, modified double-blind, placebo-controlled phase 3 trial to assess the safety and clinical efficacy of M-001, an influenza vaccine administered intramuscularly tw... | |||||||||||||
Medical condition: Flu vaccination | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) LV (Completed) BG (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005708-17 | Sponsor Protocol Number: ELB139202-05 | Start Date*: 2006-03-27 | |||||||||||
Sponsor Name:elbion AG | |||||||||||||
Full Title: International, multicenter, randomized, double-blind, placebo controlled, two-period, cross-over study to demonstrate safety, tolerability and anxiolytic effects of 600 mg ELB139 given orally t.i.d... | |||||||||||||
Medical condition: Male and female patients with diagnosis of concurrent panic disorder according to DSM-IV, with or without agoraphobia (DSM IV 300.21 and 300.1) according to Mini International Neuropsychiatric Inte... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003524-20 | Sponsor Protocol Number: BP41316 | Start Date*: 2020-12-15 | |||||||||||
Sponsor Name:F. HOFFMANN - LA ROCHE LTD. | |||||||||||||
Full Title: A phase II multicenter, randomized, double-blind, 12-week treatment, 3-arm, parallel-group, placebo-controlled study to investigate the efficacy, safety and tolerability of RO7017773 in participant... | |||||||||||||
Medical condition: Autism Spectrum Disorder (ASD) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003989-12 | Sponsor Protocol Number: NBI-1065845-MDD2024 | Start Date*: 2022-04-06 | ||||||||||||||||
Sponsor Name:Neurocrine Biosciences, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Adjunctive NBI-1065845 in Adult Subjects With Major Depressive Disorder (MDD) | ||||||||||||||||||
Medical condition: Major Depressive Disorder (MDD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) SK (Completed) BG (Completed) PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000576-33 | Sponsor Protocol Number: RBN 542 | Start Date*: 2006-06-13 |
Sponsor Name:St Helens & Knowsley Hospitals NHS Trust [...] | ||
Full Title: Pilot Study to investigate the role of Glutamine in the early protective stress response | ||
Medical condition: Critical Illness | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002778-30 | Sponsor Protocol Number: GR-2018-12367476 | Start Date*: 2022-01-12 | |||||||||||
Sponsor Name:IRCCS, OSPEDALE PEDIATRICO BAMBINO GESÙ DI ROMA | |||||||||||||
Full Title: Efficacy and safety of memantine as antimanic and mood-stabilizing medication for adolescents with Bipolar Disorder: a multi-center, randomized, double-blind, placebo-controlled clinical trial | |||||||||||||
Medical condition: Bipolar Disorder | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004291-18 | Sponsor Protocol Number: 54135419TRD4010 | Start Date*: 2021-04-08 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: Open-label Long-Term Extension Study for Participants With Treatment-Resistant Major Depressive Disorder Who are Continuing Esketamine Nasal Spray Treatment From Study 54135419TRD3013 | |||||||||||||
Medical condition: Treatment-Resistant Major Depressive Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) CZ (Completed) HU (Completed) PL (Completed) BG (Completed) FI (Completed) GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012876-29 | Sponsor Protocol Number: 10762 | Start Date*: 2009-07-07 |
Sponsor Name:University Hospitals Leicester | ||
Full Title: A prospective study to assess emergence and transmissibility of drug resistance to neuraminidase inhibitor following treatment of children and adults with acute pandemic influenza | ||
Medical condition: Influenza | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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