- Trials with a EudraCT protocol (167)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
167 result(s) found for: Community Health.
Displaying page 1 of 9.
EudraCT Number: 2015-001239-19 | Sponsor Protocol Number: PHRN14-PFD-CAPE_COD | Start Date*: 2015-08-14 | |||||||||||
Sponsor Name:CHRU de TOURS | |||||||||||||
Full Title: Effects of low-dose corticosteroids on survival of severe Community-Acquired Pneumonia | |||||||||||||
Medical condition: Severe community-acquired pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002871-15 | Sponsor Protocol Number: V58P13 | Start Date*: 2007-09-14 |
Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | ||
Full Title: A Phase III, Randomized, Observer-Blind, Placebo-Controlled, Multicenter Study to Assess Clinical Efficacy of a Cell-Derived Subunit Influenza Vaccine and an Egg-Derived Subunit Influenza Vaccine i... | ||
Medical condition: Influenza disease. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-022380-35 | Sponsor Protocol Number: 982 | Start Date*: 2011-06-10 | |||||||||||
Sponsor Name:Biotest AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter, parallel-group, adaptive group-sequential phase II study, to determine the efficacy and safety of BT086 as an adjunctive treatment in ... | |||||||||||||
Medical condition: severe Community Acquired Pneumonia (sCAP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006951-32 | Sponsor Protocol Number: REP0321 | Start Date*: 2022-04-05 | |||||||||||
Sponsor Name:Dompé farmaceutici s.p.a. | |||||||||||||
Full Title: Reparixin 1200 mg three times a day as add-on therapy to standard of care to limit disease progression in hospitalised adult patients with COVID-19 and other community-acquired pneumonia. A multina... | |||||||||||||
Medical condition: COVID-19 and other community-acquired pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) IT (Ongoing) DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004071-13 | Sponsor Protocol Number: PTK0796-CABP-1200 | Start Date*: 2015-05-20 | |||||||||||
Sponsor Name:Paratek Pharma LLC | |||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind, Multi-Center Study to Compare the Safety and Efficacy of Omadacycline IV/PO to Moxifloxacin IV/PO for Treating Adult Subjects with Community-Acquired Bacterial P... | |||||||||||||
Medical condition: Community-Acquired Bacterial Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) HU (Completed) CZ (Completed) LV (Completed) DE (Completed) ES (Completed) BE (Completed) PL (Prematurely Ended) GR (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002177-34 | Sponsor Protocol Number: 10 150 02 | Start Date*: 2013-11-07 | |||||||||||
Sponsor Name:CHU de Toulouse | |||||||||||||
Full Title: Population pharmacokinetics of levofloxacin in intensive care patients with severe community-acquired pneumonia | |||||||||||||
Medical condition: community-acquired pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003244-27 | Sponsor Protocol Number: PANORAMIC-Norway | Start Date*: 2023-04-11 | ||||||||||||||||
Sponsor Name:Helse Bergen HF | ||||||||||||||||||
Full Title: PAxlovid loNg cOvid-19 pRevention triAl with recruitMent In the Community in Norwayy | ||||||||||||||||||
Medical condition: COVID-19 SARS-CoV-2 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NO (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000736-37 | Sponsor Protocol Number: 1001 | Start Date*: 2022-08-12 | ||||||||||||||||
Sponsor Name:Biotest AG | ||||||||||||||||||
Full Title: A randomized, placebo-controlled, double-blind, multi-center, phase III trial to assess the efficacy and safety of trimodulin (BT588) in adult hospitalized subjects with CAP including COVID-19 pneu... | ||||||||||||||||||
Medical condition: non-severe community-acquired pneumonia (CAP) or moderate or severe Coronavirus Disease 2019 (COVID-19) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Ongoing) ES (Prematurely Ended) HU (Completed) AT (Ongoing) BE (Ongoing) LV (Ongoing) LT (Ongoing) PT (Ongoing) SK (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003444-37 | Sponsor Protocol Number: ENTERR06929 | Start Date*: 2016-08-26 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Bacillus clausii in the treatment of acute community–acquired diarrhea among Latin American children (cadiLAc) | |||||||||||||
Medical condition: Diarrhea | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001873-10 | Sponsor Protocol Number: P160929J | Start Date*: 2020-04-03 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS | |||||||||||||
Full Title: ANTIBIOTIC THERAPY IN RESPIRATORY TRACT INFECTIONS: AIR. A controlled randomized, open label, multicenter, non-inferiority trial evaluating an individualized antibiotic duration treatment strategy ... | |||||||||||||
Medical condition: Community acquired pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002120-14 | Sponsor Protocol Number: 3074K4-2207-WW | Start Date*: 2008-10-29 | |||||||||||||||||||||
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceutical Inc. | |||||||||||||||||||||||
Full Title: A Multicenter, Open-Label, Ascending Multiple-Dose Study to Assess the Pharmacokinetics, Safety, and Tolerability of Tigecycline in Patients 8 to 11 Years of Age With Selected Serious Infections | |||||||||||||||||||||||
Medical condition: Complicated intra-abdominal infections (cIAI), complicated skin and skin structure infections (cSSSI), community-acquired pneumonia (CAP). | |||||||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) GB (Completed) Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-004039-37 | Sponsor Protocol Number: CE01-203 | Start Date*: 2014-10-10 |
Sponsor Name:Cempra Pharmaceuticals, Inc. | ||
Full Title: A Phase 2/3, Randomised, Partly blinded (blinded investigator), Multi-center, Comparative Study to Determine the Safety and activity of Solithromycin (Intravenous and oral) in paediatric patients ... | ||
Medical condition: suspected or confirmed community acquired bacterial pneuumonia (CABP) | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA GB (Completed) HU (Completed) ES (Temporarily Halted) | ||
Trial results: View results |
EudraCT Number: 2012-002203-18 | Sponsor Protocol Number: P903-31 | Start Date*: 2012-07-18 | ||||||||||||||||||||||||||
Sponsor Name:Cerexa, Inc. (subsidary of Forest Laboratories) | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Observer-Blinded, Active-Controlled Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of Ceftaroline Versus Ceftriaxone in Pediatric Subjects With... | ||||||||||||||||||||||||||||
Medical condition: Community-acquired Bacterial Pneumonia | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA HU (Completed) GR (Completed) ES (Completed) PL (Completed) BG (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003628-29 | Sponsor Protocol Number: REGC-15-035.R1 | Start Date*: 2015-12-01 |
Sponsor Name:University of Brighton | ||
Full Title: The introduction and use of Entonox as an alternative method of pain relief for intrauterine contraception device insertions. | ||
Medical condition: This study is to investigate the efficacy of 2 methods of pain relief during the procedure of an intrauterine contraceptive device insertion (coil). There is no medical condition or disease under i... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-001731-55 | Sponsor Protocol Number: 106636 | Start Date*: 2007-08-09 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A phase III/IV, community-randomized, controlled study to evaluate the effectiveness of two vaccination strategies using GlaxoSmithKline Biologicals’ HPV-16/18 L1 VLP AS04 vaccine in reducing the p... | |||||||||||||
Medical condition: For the prevention of high-grade cervical intraepithelial neoplasia (CIN grades 2 and 3) and cervical cancer causally related to human papillomavirus (HPV) types 16 and 18. | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004425-27 | Sponsor Protocol Number: 5863 | Start Date*: 2012-05-29 |
Sponsor Name:Newcastle Upon Tyne Hospitals NHS Foundation Trust | ||
Full Title: Study of Optimal Replacement of Thyroxine in the ElDerly (SORTED) SORTED 1 – a Randomised Controlled Trial (Pilot study) SORTED 2 – Qualitative Interviews SORTED 3 – Retrospective Cohort | ||
Medical condition: hypothyroidism (elderly individuals) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002612-25 | Sponsor Protocol Number: versie 2 | Start Date*: 2007-09-14 | |||||||||||
Sponsor Name:St. Antonius Hospital | |||||||||||||
Full Title: Dexamethasone infusion in community-acquired pneumonia | |||||||||||||
Medical condition: pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003932-35 | Sponsor Protocol Number: BIO101-CL03 | Start Date*: 2018-02-20 | |||||||||||
Sponsor Name:Biophytis S.A. | |||||||||||||
Full Title: Safety and Efficacy of BIO-101 175 mg b.i.d. and 350 mg b.i.d. 26-week oral administration to patients suffering from age-related SARcopenia, including sarcopenic obesity, Aged ≥65 years and at ris... | |||||||||||||
Medical condition: Sarcopenia including sarcopenic obesity | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001637-41 | Sponsor Protocol Number: A7801001 | Start Date*: 2005-07-26 |
Sponsor Name:Pfizer Consumer Healthcare cva/sca | ||
Full Title: A community pharmacy based investigation in the self-medication area Efficacy and safety of Sinutab® (Paracetamol (500mg)/Pseudoephedrine (30mg)) on subjects with nasal congestion accompanied by h... | ||
Medical condition: Medical rationale= Investigation of combination drug Sinutab in symptomatic relief of common cold with nasal symptoms. Community pharmacists are considered as local investigators including subjec... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000058-35 | Sponsor Protocol Number: A7801002 | Start Date*: 2006-04-26 |
Sponsor Name:Pfizer Consumer Healthcare Comm. VA/SCA | ||
Full Title: A community pharmacy based investigation in the self-medication area Efficacy and safety of Sinutab® [Paracetamol (500mg) and Pseudoephedrine (30mg)] on subjects with nasal congestion accompanied ... | ||
Medical condition: The medical rationale = to investigate this combination drug in the symptomatic relief of common cold with nasal symptoms. The reduction of symptom severity may allow subjects receiving active medi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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