- Trials with a EudraCT protocol (34)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (735)
34 result(s) found for: Fluconazole.
Displaying page 1 of 2.
EudraCT Number: 2021-006868-24 | Sponsor Protocol Number: UMCN-AKF-21.05 | Start Date*: 2022-08-02 | |||||||||||
Sponsor Name:Radboud university medical centre | |||||||||||||
Full Title: Pharmacokinetics of fluconazole given orally or intravenously as prophylaxis or therapy to children and adolescents with invasive fungal infections (FOCUS) | |||||||||||||
Medical condition: Invasive fungal disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001916-41 | Sponsor Protocol Number: C11-11 | Start Date*: 2014-11-24 |
Sponsor Name:Inserm | ||
Full Title: Fluconazole versus Micafungin in neonates with suspected or culture-proven Candidiasis: a randomized pharmacokinetic and safety study | ||
Medical condition: Neonates with suspected or culture-proven candidiasis | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) IT (Prematurely Ended) NL (Completed) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001585-15 | Sponsor Protocol Number: 2018-01671 | Start Date*: 2020-01-30 |
Sponsor Name:Centre Hospitalier Universitaire Vaudois | ||
Full Title: PTX3 genetically stratified randomized double-blinded allocation eventdriven clinical trial for antifungal prophylaxis in patients with acute myeloid leukemia | ||
Medical condition: Patients with acute myeloid leukemia (AML) or myelodysplastic syndrome in transformation (MDSit) who receive antifungal profylaxis during their treatment with an intensive chemotherapy regimen, inc... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003172-39 | Sponsor Protocol Number: Mica1/2012 | Start Date*: 2013-05-23 |
Sponsor Name:Medizinische Universität Innsbruck, Abteilung für Hygiene und Medizinische Mikrobiologie | ||
Full Title: Micafungin-Deescaltion study: Evalutating the rate of breakthrough infections of micafungin followed by fluconazole versus fluconazole (or other azoles) in febrile patients | ||
Medical condition: All patients who are suspicious of suffering from invasive fungal infections are included. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003611-21 | Sponsor Protocol Number: 2013-003611-21 | Start Date*: 2013-12-20 | ||||||||||||||||
Sponsor Name:Karolinska Institutet | ||||||||||||||||||
Full Title: Safety of fluconazol treatment of premature and full-term newborns - a study on interactions by NSAIDs with fluconazole in respect of pharmacodynamic endpoints with urinary excretion of vas... | ||||||||||||||||||
Medical condition: Fungal infection prophylaxis Patent ductus arteriosus | ||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002271-97 | Sponsor Protocol Number: F901318C21 | Start Date*: 2017-04-07 | |||||||||||
Sponsor Name:F2G Limited | |||||||||||||
Full Title: An open label phase IIa clinical study to evaluate the safety and pharmacokinetics of oral F901318 (combined with fluconazole and posaconazole) for antifungal prophylaxis in patients undergoing che... | |||||||||||||
Medical condition: Invasive fungal disease in patients with acute myeloid leukemia under chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003541-15 | Sponsor Protocol Number: 2019-Fungi | Start Date*: 2020-02-19 | |||||||||||
Sponsor Name:Aarhus University | |||||||||||||
Full Title: Adjunct effect of fluconazole in the treatment of Candida-associated refractory severe periodontitis – A single-center, placebo-controlled, triple blind, randomized clinical trial | |||||||||||||
Medical condition: Periodontitis. The participants are in good general health, but have at least 2 residual dental lesions after periodontal treatment (standard care). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002613-35 | Sponsor Protocol Number: UMCN-AKF-18.07 | Start Date*: 2018-11-05 | |||||||||||
Sponsor Name:Radboud university medical centre | |||||||||||||
Full Title: Fluconazole pharmacokinetics, including bioavailability, in Obese subjects after an Intravenous and oral Administration (FOLIA). | |||||||||||||
Medical condition: Pharmacokinetics of fluconazole in obese subjects. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002204-38 | Sponsor Protocol Number: NDI-2020 | Start Date*: 2020-11-24 | |||||||||||
Sponsor Name:Claus Bistrup | |||||||||||||
Full Title: Treatment of congenital nephrogenic diabetes insipidus with fluconazole, an antifungal medication | |||||||||||||
Medical condition: Nephrogenic diabetes insipidus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000648-32 | Sponsor Protocol Number: SCY-078-302 | Start Date*: 2023-03-31 | ||||||||||||||||
Sponsor Name:SCYNEXIS, Inc. | ||||||||||||||||||
Full Title: A Phase 3, Multicenter, Prospective, Randomized, Double-blind Study of Two Treatment Regimens for Candidemia and/or Invasive Candidiasis: Intravenous Echinocandin followed by Oral Ibrexafungerp ver... | ||||||||||||||||||
Medical condition: Invasive Candidiasis/ Candidemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Trial now transitioned) FR (Trial now transitioned) ES (Temporarily Halted) BE (Trial now transitioned) BG (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003011-97 | Sponsor Protocol Number: 69HCL20_0071 | Start Date*: 2020-12-14 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Fluconazole as a new therapeutic tool in hypercalciuric patients with increased 1,25(OH)2D levels. | |||||||||||||
Medical condition: Hypercalciuria | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005599-51 | Sponsor Protocol Number: CD101.IV.2.03 | Start Date*: 2016-09-26 | |||||||||||
Sponsor Name:Cidara Therapeutics Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Double-blind Study of the Safety, Tolerability, and Efficacy of CD101 Injection vs Intravenous Caspofungin Followed By Oral Fluconazole Step-down in the Treatmen... | |||||||||||||
Medical condition: Candidemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GR (Completed) HU (Completed) BG (Completed) BE (Completed) IT (Completed) RO (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 (Trial now transitioned) BE (Trial now transitioned) NL (Ongoing) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-004192-16 | Sponsor Protocol Number: 3.0 | Start Date*: 2023-04-12 | ||||||||||||||||
Sponsor Name:idival | ||||||||||||||||||
Full Title: Evaluation of the efficacy of treatment with mucosal bacterial vaccines (autovaccines) versus suppressive antibiotic treatment in subjects with hip or knee prosthesis infections. | ||||||||||||||||||
Medical condition: Patients with chronic infections of hip and knee prostheses, without the possibility of curative treatment of the infection. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004398-22 | Sponsor Protocol Number: 1 | Start Date*: 2013-07-01 |
Sponsor Name:Afd. A, OUH | ||
Full Title: intraperitoneal microdialysis after server peritonitis | ||
Medical condition: server peritonitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-006011-23 | Sponsor Protocol Number: 130669 | Start Date*: 2021-03-02 |
Sponsor Name:Petra Pietarinen | ||
Full Title: Laryngeaalisen leukoplakian mikrobilääkehoito -tutkimusprojekti | ||
Medical condition: Krooninen laryngiitti | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: | |
Trial protocol: FI (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000758-81 | Sponsor Protocol Number: Chlorhex-KKDS-2021 | Start Date*: 2021-04-08 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Chlorhexidine gluconate as treatment and prophylaxis of vulvovaginal Candidiasis | ||
Medical condition: Candida vulvovaginitis | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000925-27 | Sponsor Protocol Number: ProF-001_Phase_IIb/III | Start Date*: 2019-08-27 | |||||||||||
Sponsor Name:Profem GmbH | |||||||||||||
Full Title: A phase IIb/III, parallel-arm, randomized, active-controlled, double-blind, double-dummy, study in patients with recurrent vulvovaginal candidiasis to compare the clinical efficacy, safety and tole... | |||||||||||||
Medical condition: recurrent vulvovaginal candidiasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002587-28 | Sponsor Protocol Number: 2019-5165 | Start Date*: 2020-02-25 |
Sponsor Name:Radboudumc | ||
Full Title: ABSORB 2:An exploratie study determining the oral antibiotic drug absorption in patients with short bowel syndrome. | ||
Medical condition: short bowel syndrome, home parenteral nutrition | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002630-21 | Sponsor Protocol Number: CD101.IV.3.05 | Start Date*: 2019-01-10 | ||||||||||||||||
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 Intravenous Caspofungin Followed by Optional Oral Fluconazole Step-down in the... | ||||||||||||||||||
Medical condition: Candidemia; invasive candidiasis. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) DE (Completed) GR (Completed) FR (Completed) BE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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