- Trials with a EudraCT protocol (179)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (33)
179 result(s) found for: Lower Respiratory Tract Infection.
Displaying page 1 of 9.
| EudraCT Number: 2008-006435-13 | Sponsor Protocol Number: 5065 | Start Date*: 2008-10-15 | ||||||||||||||||
| Sponsor Name:University of Southampton | ||||||||||||||||||
| Full Title: GRACE (Genomics to combat Resistance against Antibiotics in Community-acquired LRTI in Europe).Workpackage 10: Antibiotic Trial One | ||||||||||||||||||
| Medical condition: Lower Respiratory Tract Infection | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SI (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2007-001586-15 | Sponsor Protocol Number: 5065 | Start Date*: 2007-10-16 | ||||||||||||||||
| Sponsor Name:University of Southampton | ||||||||||||||||||
| Full Title: GRACE (Genomics to combat Resistance against Antibiotics in Community-acquired LRTI in Europe).Workpackage 10: Antibiotic Trial One | ||||||||||||||||||
| Medical condition: Lower Respiratory Tract Infection | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) GB (Completed) BE (Completed) SE (Completed) ES (Completed) IT (Completed) DE (Completed) FR (Completed) SK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-002705-19 | Sponsor Protocol Number: OMPeR | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO | |||||||||||||
| Full Title: A phase IV, randomized, controlled, double-blind study on efficacy and safety of OM-85 in children with recurrent respiratory tract infections | |||||||||||||
| Medical condition: Recurrent Respiratory Tract Infection | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001882-36 | Sponsor Protocol Number: ACHIEVE | Start Date*: 2020-05-07 | |||||||||||
| Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
| Full Title: ANTI-INFLAMMATORY CLARITHROMYCIN TO IMPROVE SARS-CoV-2 (COVID-19) INFECTION EARLY: THE ACHIEVE OPEN-LABEL NON-RANDOMIZED CLINICAL TRIAL | |||||||||||||
| Medical condition: Management of infection by SARS-CoV-2 (COVID-19) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-005740-83 | Sponsor Protocol Number: 4825 | Start Date*: 2007-01-12 | |||||||||||
| Sponsor Name:University of Southampton | |||||||||||||
| Full Title: A Pragmatic Randomised Trial of Ibuprofen, Paracetamol, Steam and Delayed Prescribing for Patients with Respiratory Tract Infections in Primary Care | |||||||||||||
| Medical condition: Inclusion criteria Patients aged 3 to 65 presenting to a GP or nurse with an RTI (acute cold, influenza, sore throat, otitis media, sinusitis, croup, or lower respiratory tract infection). Exclus... | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002733-22 | Sponsor Protocol Number: MB0515/1021/03 | Start Date*: 2015-09-09 | |||||||||||
| Sponsor Name:VALEAS SPA - INDUSTRIA CHIMICA E FARMACEUTICA | |||||||||||||
| Full Title: Combined treatment with pidotimod and bifidobacteria in pre-scholastic age children with recurrent respiratory infections: evaluation of clinical efficacy and parents' quality of life | |||||||||||||
| Medical condition: Recurrent respiratory infections | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001651-49 | Sponsor Protocol Number: ALX0171-C201 | Start Date*: 2016-11-07 | |||||||||||
| Sponsor Name:Ablynx NV | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, multicenter dose ranging study of ALX-0171 in infants and young children hospitalized for respiratory syncytial virus lower respiratory tract infection | |||||||||||||
| Medical condition: RSV lower respiratory tract infection | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) LV (Completed) HU (Completed) ES (Completed) EE (Completed) LT (Completed) SK (Completed) BE (Completed) BG (Completed) CZ (Completed) Outside EU/EEA PL (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000886-42 | Sponsor Protocol Number: BV-2020/08 | Start Date*: 2022-09-06 | |||||||||||
| Sponsor Name:OM Pharma SA | |||||||||||||
| Full Title: A Randomised, Placebo-Controlled, 3-Arm, Double-Blind, Multicentre, Phase 4 Study to Assess the Efficacy of OM-85 (Broncho Vaxom) Short- and Long-Term Treatment vs. Placebo in the Prevention of Res... | |||||||||||||
| Medical condition: Respiratory Tract Infections with Wheezing Lower Respiratory Illness | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021422-35 | Sponsor Protocol Number: 09-NI-EP-001 | Start Date*: 2010-10-26 | |||||||||||
| Sponsor Name:Deutsche Homöopathie-Union, DHU-Arzneimittel GmbH & Co. KG | |||||||||||||
| Full Title: Efficacy, safety and tolerability of Influcid tablets in patients (1 to 65 years old) suffering from upper respiratory tract infections with flu-like symptoms. A randomized, international, multicen... | |||||||||||||
| Medical condition: Diagnosed upper respiratory tract infection (URTI) with presence of the following symptoms for equal or less than for 24 hours : a)Fever (axillary temperature >= 37.5°C) and b)At least one upper ... | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001345-38 | Sponsor Protocol Number: UNIKINON-01/HOPE | Start Date*: 2020-04-02 | |||||||||||
| Sponsor Name:Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories S.A. | |||||||||||||
| Full Title: CHROLOQUINE PHOSPHATE AGAINST INFECTION BY THE NOVEL CORONAVIRUS SARS-CoV-2 (COVID-19): THE HOPE OPEN-LABEL, NON-RANDOMIZED CLINICAL TRIAL | |||||||||||||
| Medical condition: Possible prevention of pneumonia from SARS-CoV-2 in patients staying home and improving symptoms of SARS-CoV-2 pneumonia in patients treated in hospital | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005187-25 | Sponsor Protocol Number: BUC-SI-11-001 | Start Date*: 2012-05-31 | |||||||||||
| Sponsor Name:SOCIETA' LABORATORIO FARMACEUTICO S.I.T. SRL | |||||||||||||
| Full Title: Efficacy and tolerability clinical trial of an immunostimulant made from inactivated bacteria (BUCCALIN) in the prophylaxis of infection of the airways (rhinotracheobronchitis, colds). Double-blind... | |||||||||||||
| Medical condition: Episodes classified by upper respiratory infections (otitis, tonsillitis, sinusitis, pharyngotonsillitis, nasopharyngitis) and lower respiratory tract (bronchitis, pneumonia). | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005980-30 | Sponsor Protocol Number: 53718678RSV2008 | Start Date*: 2021-11-26 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Phase 2b Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Rilematovir (JNJ-53718678) in Adult Outpatients with Respiratory Syncytial Virus (RSV) Infection... | |||||||||||||
| Medical condition: Respiratory Syncytial Virus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DE (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) PL (Completed) HU (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001325-31 | Sponsor Protocol Number: NL73551.091.20 | Start Date*: 2020-05-20 | |||||||||||||||||||||
| Sponsor Name:Radboud University Medical Center | |||||||||||||||||||||||
| Full Title: [68Ga]Ga-DOTA-(RGD)2 PET/CT imaging of activated endothelium in lung parenchyma of COVID-19 patients. | |||||||||||||||||||||||
| Medical condition: Maximum 10 patients from the Infectious Diseases ward with proven COVID-19 infection and pulmonary abnormalities on contrast-enhanced CT undergo static PET scans after injection of 70 μg (200 MBq) ... | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2014-002475-29 | Sponsor Protocol Number: GS-US-218-1502 | Start Date*: 2015-02-10 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Multi-Center Study Evaluating Antiviral Effects, Pharmacokinetics, Safety, and Tolerability of GS-5806 in Hematopoietic Cell Transplant (HCT... | |||||||||||||
| Medical condition: Respiratory Syncytial Virus (RSV) Infection of the lower respiratory tract. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002474-36 | Sponsor Protocol Number: GS-US-218-0108 | Start Date*: 2014-11-24 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Multi-Center Study Evaluating Antiviral Effects, Pharmacokinetics, Safety, and Tolerability of GS-5806 in Hematopoietic Cell Transplant (HCT... | |||||||||||||
| Medical condition: Respiratory Syncytial Virus (RSV) Infection of the upper respiratory tract. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DE (Completed) GB (Completed) NL (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000825-33 | Sponsor Protocol Number: MI-CP117 | Start Date*: 2012-03-09 | |||||||||||
| Sponsor Name:MedImmune LLC | |||||||||||||
| Full Title: A Phase 3 Study of MEDI-524 (Motavizumab) for the Prevention of RSV Disease Among Native American Infants in the Southwestern United States | |||||||||||||
| Medical condition: Serious Lower Respiratory Tract disease caused by RSV | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002093-31 | Sponsor Protocol Number: T47151 | Start Date*: 2012-05-03 |
| Sponsor Name:Oulu University Hospital | ||
| Full Title: Diagnosis community-acquired pneumonia in emergency unit | ||
| Medical condition: lower respiratory tract infection and pneumonia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002302-39 | Sponsor Protocol Number: RSV-M-301 | Start Date*: 2016-09-06 | |||||||||||
| Sponsor Name:Novavax, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Observer-Blind, Placebo-Controlled, Group-Sequential Study to Determine the Immunogenicity and Safety of a Respiratory Syncytial Virus (RSV) F Nanoparticle Vaccine with Alumi... | |||||||||||||
| Medical condition: Respiratory syncytial virus (RSV) is the leading viral cause of severe lower respiratory tract disease in infants and young children worldwide. In industrialized countries, nearly all children have... | |||||||||||||
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| Population Age: In utero, Newborns, Infants and toddlers, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002137-58 | Sponsor Protocol Number: GS-US-218-1227 | Start Date*: 2014-09-29 | |||||||||||
| Sponsor Name:Gilead Sciences Inc | |||||||||||||
| Full Title: A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Multi-Center Study Evaluating Antiviral Effects, Pharmacokinetics, Safety, and Tolerability of GS-5806 in Hospitalized Adults with Respirato... | |||||||||||||
| Medical condition: Respiratory Syncytial Virus (RSV) Infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) BE (Completed) IT (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002841-23 | Sponsor Protocol Number: ALX0171-C104 | Start Date*: 2014-09-22 | |||||||||||
| Sponsor Name:Ablynx NV | |||||||||||||
| Full Title: A Phase I/IIa Multicentre Study in Otherwise Healthy Infants and Toddlers Hospitalised For and Diagnosed With Respiratory Syncytial Virus Lower Respiratory Tract Infection, Consisting of an Open-la... | |||||||||||||
| Medical condition: Respiratory Syncytial Virus Lower Respiratory Tract Infection | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) HU (Completed) SK (Completed) BE (Completed) ES (Completed) EE (Prematurely Ended) LV (Prematurely Ended) BG (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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