- Trials with a EudraCT protocol (20)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
20 result(s) found for: Sulfamethoxazole/trimethoprim.
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EudraCT Number: 2012-004424-38 | Sponsor Protocol Number: SUTRICA | Start Date*: 2013-01-29 | ||||||||||||||||
Sponsor Name:Department of Haematology, Aalborg University Hospital | ||||||||||||||||||
Full Title: A randomized, open-label phase III study of Clarithromycin, Sulfamethoxa-zole/Trimethoprim or observation in combination with standard therapy in patients with newly diagnosed multiple myeloma | ||||||||||||||||||
Medical condition: Multiple myeloma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005475-41 | Sponsor Protocol Number: MLX | Start Date*: 2014-11-05 |
Sponsor Name:UZ Brussel | ||
Full Title: Sulfamethoxazole treatment of primary PREPL deficiency | ||
Medical condition: Hypotonia-cystinuria syndrome and isolated PREPL deficiency. | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000219-25 | Sponsor Protocol Number: MRSA | Start Date*: 2013-07-18 |
Sponsor Name:AOU Meyer | ||
Full Title: Early eradication of S. Aureus (MRSA) in patients with cystic fibrosis: a randomized multicenter study. | ||
Medical condition: Patients affected by cystic fibrosis and who present an initial infection of MRSA. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005721-43 | Sponsor Protocol Number: D4280C00002 | Start Date*: 2012-05-14 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase III, Randomized, Multicenter, Double-Blind, Double Dummy, Parallel Group, Comparative Study to Determine the Efficacy, Safety, and Tolerability of Ceftazidime-Avibactam (CAZ-AVI, formerly C... | ||
Medical condition: Complicated Urinary Tract Infections (cUTIs) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) BE (Completed) BG (Completed) DE (Completed) CZ (Completed) SK (Completed) PT (Completed) HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-005627-21 | Sponsor Protocol Number: APHP211043 | Start Date*: 2022-08-31 |
Sponsor Name:APHP | ||
Full Title: 3-day intravenous antibiotic treatment versus 3-day intravenous followed by 7-day oral antibiotic treatment for acute pyelonephritis in children 1 month to 3 years old: a non-inferiority open rando... | ||
Medical condition: Acute pyelonephritis in children 1 month to 3 years old | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Suspended by CA) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005722-21 | Sponsor Protocol Number: D4280C00004 | Start Date*: 2012-06-05 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase III, Randomized, Multicenter, Double-Blind, Double Dummy, Parallel Group, Comparative Study to Determine the Efficacy, Safety, and Tolerability of Ceftazidime-Avibactam (CAZ-AVI, formerly C... | ||
Medical condition: Complicated Urinary Tract Infections (cUTIs) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) DE (Completed) CZ (Completed) ES (Completed) IT (Completed) BG (Completed) PL (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021242-22 | Sponsor Protocol Number: PHRN09-LB / DATIPO | Start Date*: 2011-07-26 | |||||||||||
Sponsor Name:CHRU de Tours | |||||||||||||
Full Title: Etude multicentrique, de non infériorité, randomisée, ouverte, évaluant l’efficacité de deux Durées d’Antibiothérapie (6 semaines versus 12 semaines) dans le Traitement des Infections sur Prothèses... | |||||||||||||
Medical condition: Infection sur prothèse ostéo-articulaire | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005215-98 | Sponsor Protocol Number: IUWP2005.01 | Start Date*: 2007-03-12 | |||||||||||
Sponsor Name:Sanquin Plasma Products | |||||||||||||
Full Title: Treatment in patients with recurrent infections and IgG Subclass Deficiency, and/or Deficient Anti-Polysaccharide Antibody Response. | |||||||||||||
Medical condition: Established diagnosis of IgG subclass deficiency, and/or (selective) antipolysaccharide antibody deficiency. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001466-11 | Sponsor Protocol Number: SAVE | Start Date*: 2020-04-15 | |||||||||||
Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
Full Title: suPAR-GUIDED ANAKINRA TREATMENT FOR VALIDATION OF THE RISK AND EARLY MANAGEMENT OF SEVERE RESPIRATORY FAILURE BY COVID-19: THE SAVE OPEN-LABEL, NON-RANDOMIZED SINGLE-ARM TRIAL | |||||||||||||
Medical condition: Lower respiratory tract infection by Covid-19 at high risk for development of severe respiratory failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004298-24 | Sponsor Protocol Number: KCH-STR-INF | Start Date*: 2008-08-13 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust [...] | |||||||||||||
Full Title: A cluster randomised trial of different strategies of antibiotic use to reduce the incidence and consequences of chest infection in acute stroke patients with swallowing problems. | |||||||||||||
Medical condition: Acute stroke patients with dysphagia and at high risk of aspiration as assessed by the bedside swallowing assessment. A policy to prevent pneumonias with prophylactic antibiotics is being investig... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005409-38 | Sponsor Protocol Number: TriSulfa-FPI-1 | Start Date*: 2013-04-19 | |||||||||||
Sponsor Name:Fundación Pública Andaluza para la Gestión de la Investigación en Salud de Sevilla (FISEVI) | |||||||||||||
Full Title: Pilot study phase III to evaluate the efficacy and safety of Trimethoprim-sulfamethoxazole in the treatment of idiopathic pulmonary fibrosis | |||||||||||||
Medical condition: Ambulatory patients, men and women, with well-established diagnosis of idiopathic pulmonary fibrosis. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022096-54 | Sponsor Protocol Number: Repha_1344 | Start Date*: 2011-04-04 | |||||||||||
Sponsor Name:Repha GmbH | |||||||||||||
Full Title: Randomised, prospective, double-dummy double-blinded study to evaluate safety and efficacy of Angocin Anti-Infekt N versus standard antibiotics in the treatment of acute uncomplicated cystitis | |||||||||||||
Medical condition: Treatment of acute uncomplicated cystitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004981-85 | Sponsor Protocol Number: CD101.IV.3.08 | Start Date*: 2020-04-06 | |||||||||||
Sponsor Name:Cidara Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind Study of the Efficacy and Safety of Rezafungin for Injection Versus the Standard Antimicrobial Regimen to Prevent Invasive Fungal Diseases in Adults... | |||||||||||||
Medical condition: Invasive Fungal Diseases in Adults undergoing Allogeneic Blood and Marrow Transplantation (BMT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) NL (Ongoing) GB (GB - no longer in EU/EEA) FR (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021241-44 | Sponsor Protocol Number: PHRI06 – LB / PACHIU | Start Date*: 2010-12-13 | |||||||||||
Sponsor Name:CHRU de TOURS | |||||||||||||
Full Title: Etude multicentrique, randomisée en groupes parallèles, évaluant l’efficacité et la tolérance d’un antibiocycle hebdomadaire dans la prévention des infections urinaires sur vessie neurologique. | |||||||||||||
Medical condition: troubles de la vessie dû à une maladie neurologique | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000309-21 | Sponsor Protocol Number: PREDICT_Trial_Amd_04 | Start Date*: 2013-10-01 | |||||||||||
Sponsor Name:Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico | |||||||||||||
Full Title: Antibiotic Prophylaxis and Renal Damage In Congenital abnormalities of the kidney and urinary Tract | |||||||||||||
Medical condition: Infants with vesicoureteral reflux grade III-V, started before the first symptomatic infection. | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) LT (Ongoing) ES (Ongoing) DE (Ongoing) SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000338-20 | Sponsor Protocol Number: MK-7655A-021 | Start Date*: 2019-06-26 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 2/3 Open-label, Randomized, Active-controlled Clinical Study to Evaluate the Safety, Tolerability, Efficacy and Pharmacokinetics of MK-7655A in Pediatric Participants From Birth to Less Tha... | |||||||||||||
Medical condition: Treatment of bacterial infections in pediatric populations | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) PL (Ongoing) Outside EU/EEA ES (Restarted) BG (Ongoing) GR (Ongoing) NO (Ongoing) EE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001024-34 | Sponsor Protocol Number: OraPAT-IE-GAMES | Start Date*: 2021-12-15 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: Oral antimicrobial treatment vs. outpatient parenteral for infective endocarditis. | |||||||||||||
Medical condition: infective endocarditis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000781-38 | Sponsor Protocol Number: PHAO2011/LB/LIZ-BONE | Start Date*: 2012-10-08 | |||||||||||
Sponsor Name:Direction de la recherche clinique du centre hospitalier universitaire de Tours, Bretonneau | |||||||||||||
Full Title: Prospective, Randomized, open label, European, multicenter study of the efficacy of the linezolid-rifampin combination versus standard of care in the treatment of Gram-positive prosthetic hip joint... | |||||||||||||
Medical condition: Hip prosthesis infected by gram-positive bacteria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000050-10 | Sponsor Protocol Number: FORMaT001 | Start Date*: 2023-01-02 | |||||||||||
Sponsor Name:University of Queensland | |||||||||||||
Full Title: Finding the Optimal Regimen for Mycobacterium abscessus Treatment | |||||||||||||
Medical condition: Mycobacterium abscessus pulmonary disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001297-63 | Sponsor Protocol Number: MLORI201 | Start Date*: 2023-04-13 |
Sponsor Name:Melinta Therapeutics, LLC | ||
Full Title: A Multicenter, Open-Label, Evaluator-Blinded, Randomized Study to Evaluate the Safety and Tolerability of Single-Dose IV Oritavancin Versus Standard of Care for the Treatment of Pediatric Subjects... | ||
Medical condition: Acute Bacterial Skin and Skin Structure Infections | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: BG (Ongoing) LT (Ongoing) LV (Ongoing) PL (Ongoing) ES (Ongoing) PT (Ongoing) | ||
Trial results: (No results available) |
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