- Trials with a EudraCT protocol (517)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (91)
517 result(s) found for: Urinary tract.
Displaying page 1 of 26.
EudraCT Number: 2016-004486-37 | Sponsor Protocol Number: 59812 | Start Date*: 2017-09-19 | ||||||||||||||||
Sponsor Name:University Medical Centre Utrecht | ||||||||||||||||||
Full Title: FOsfomycin Randomised controlled trial for E.coli Complicated urinary tract infections as Alternative Stepdown Treatment | ||||||||||||||||||
Medical condition: Acute febrile urinary tract infection | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005559-19 | Sponsor Protocol Number: FUR-03-17 | Start Date*: 2021-02-23 | ||||||||||||||||||||||||||
Sponsor Name:ADAMED Pharma S.A. | ||||||||||||||||||||||||||||
Full Title: FRUTI - a phase III, randomized, multicenter, double-blind, active control study to evaluate the efficacy and safety of Furazidin prolonged-release tablets, 200 mg compared with Nitrofurantoin prol... | ||||||||||||||||||||||||||||
Medical condition: uncomplicated lower urinary tract infections (acute or recurrent) | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: PL (Completed) HU (Completed) DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000963-54 | Sponsor Protocol Number: FUR-PKPD-05-20 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Adamed Pharma S.A. | ||||||||||||||||||||||||||||
Full Title: Effectiveness and pharmacokinetic /pharmacodynamic study of Furazidin, prolonged- release tablets, 200 mg in the treatment of patients with uncomplicated lower urinary tract infections (acute or re... | ||||||||||||||||||||||||||||
Medical condition: uncomplicated lower urinary tract infections (acute or recurrent) | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: PL (Prematurely Ended) DE (Prematurely Ended) HU (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002390-13 | Sponsor Protocol Number: notapplicable | Start Date*: 2009-04-08 | |||||||||||
Sponsor Name:University Hospital | |||||||||||||
Full Title: Are cranberry capsules useful in preventing urinary tract infection in hip fracture patients with urinary tract catheter | |||||||||||||
Medical condition: Urinary tract infections in patients with hip fractures. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004594-82 | Sponsor Protocol Number: CSU11001 | Start Date*: 2012-01-17 | ||||||||||||||||
Sponsor Name:Schur Pharmazeutika GmbH & Co. KG | ||||||||||||||||||
Full Title: Efficacy of an intravesical instillation with neomycin solution in acute cystitis: a double-blind, placebo-controlled trial in patients with permanent intravesical catheter | ||||||||||||||||||
Medical condition: Treatment of urinary tract infection | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005112-37 | Sponsor Protocol Number: J&P 01/2007 draft4 | Start Date*: 2008-08-21 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Abteilung für Interne Medizin I | |||||||||||||
Full Title: An randomized, controlled, investigator-blinded, prospective, mono-centre study to evaluate the efficacy of fosfomycin versus meropenem in patients with complicated urinary tract infections | |||||||||||||
Medical condition: This study will primarily address the question of the efficacy of intravenous fosfomycin 4 g b.i.d. in the therapy of patients presenting with complicated urinary tract infection. These data will b... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001427-30 | Sponsor Protocol Number: 276046 | Start Date*: 2016-06-28 | |||||||||||
Sponsor Name:University of Helsinki / CLUE Working Group | |||||||||||||
Full Title: Antibiotic prophylaxis before extracorporeal shock wave lithotripsy (APPEAL) | |||||||||||||
Medical condition: Prevention of urinary tract infections among patients undergoing extracorporeal shock wave lithotripsy for urinary stone disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001481-42 | Sponsor Protocol Number: ITFE-2026-C11 | Start Date*: 2018-10-04 | |||||||||||
Sponsor Name:ITF RESEARCH PHARMA S.L.U. | |||||||||||||
Full Title: Prospective, multicentre, randomized, double-blind, placebo-controlled clinical trial to evaluate the efficacy of a 0.005% estriol vaginal gel in the prevention of recurrent urinary tract infection... | |||||||||||||
Medical condition: Recurrent Urinary Tract Infection (UTI) in postmenopausal women with vaginal atrophy. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005912-41 | Sponsor Protocol Number: TMO-07001 | Start Date*: 2010-05-04 | ||||||||||||||||
Sponsor Name:Belpharma SA/NV | ||||||||||||||||||
Full Title: Temocillin use in Complicated Urinary Tract Infections due to ESBL producing and AmpC hyperproducing Enterobacteriaceae in United Kingdom | ||||||||||||||||||
Medical condition: Patients presenting urinary tract infections due to Extended Spectrum Beta-Lactamases producing or AmpC hyperproducing Enterobacteriaceae. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012696-97 | Sponsor Protocol Number: IGG-PNA IVU-01 | Start Date*: 2009-07-02 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Management of children following acute pyelonefritis or recurrent urinary tract infection episodes and prevention of renal scarring: a prospective randomised controlled clinical trial. | |||||||||||||
Medical condition: URINARY TRACT INFECTION | |||||||||||||
|
|||||||||||||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004397-62 | Sponsor Protocol Number: PI070274 | Start Date*: 2008-11-28 | |||||||||||
Sponsor Name:Servicio Andaluz de Salud | |||||||||||||
Full Title: Análisis aleatorizado y doble ciego sobre la utilidad del extracto de arándano rojo vs profilaxis antibiótica con Trimetoprima en la infección urinaria recurrente infantil | |||||||||||||
Medical condition: First clinical assay so far where the convenience is evaluated of carrying out prophylaxis of the pediatric urinary recurrent infection in the childhood with extract of cranberries (with a fixed co... | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002271-42 | Sponsor Protocol Number: 20110512-BG | Start Date*: 2011-10-13 | |||||||||||
Sponsor Name:University Medical Center Goettingen | |||||||||||||
Full Title: | |||||||||||||
Medical condition: uncomplicated urinary tract infection | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005552-41 | Sponsor Protocol Number: ALADIN | Start Date*: 2006-02-20 | |||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
Full Title: Effect of long-acting somatostatin on disease progression in nephropathy due to autosomal dominant polycystic disease a long-term three year follow-up study | |||||||||||||
Medical condition: Autosomal Dominant Polycystic Kidney Disease ADPKD | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024023-25 | Sponsor Protocol Number: Nefrovid2010 | Start Date*: 2011-09-22 | |||||||||||
Sponsor Name:Lorenzo Victor, PhD | |||||||||||||
Full Title: An open label, parallel groups, phase III, clinical trial to assess the antiproteinuric effects of the vitamin D derivates in patients with chronic kidney disease and vitamin D insufficiency. | |||||||||||||
Medical condition: | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002470-23 | Sponsor Protocol Number: 2011-002470-23 | Start Date*: 2011-06-09 | |||||||||||||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO MEDITERRANEO NEUROMED | |||||||||||||||||||||||
Full Title: Evaluation of diagnosic accuracy of 18F-choline PET/CT in examination of patients qith prostate cancer, in relation to PSA value and its derivatives. | |||||||||||||||||||||||
Medical condition: Patients with prostate cancer histologically proved | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006557-25 | Sponsor Protocol Number: RAPYD-STUDY | Start Date*: 2007-12-20 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: RAPAMYCIN FOR TREATMENT OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE | |||||||||||||
Medical condition: ADPKD type I | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000708-14 | Sponsor Protocol Number: ONC-RCC-02 | Start Date*: 2012-10-05 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
Full Title: A randomized, open label, multicenter phase 2 study, to evaluate the efficacy of Sorafenib in patients with advanced Renal Cell Carcinoma (RCC) after a radical resection of the metastases. | |||||||||||||
Medical condition: Advanced metastatic resected renal cell carcinoma | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003337-24 | Sponsor Protocol Number: 180 | Start Date*: 2013-06-26 | ||||||||||||||||
Sponsor Name:CENTRO DI RIFERIMENTO ONCOLOGICO DI BASILICATA | ||||||||||||||||||
Full Title: Diagnostic imaging in prostate cancer (as in tumours with accelerated menbrane turn-over)by F-18 Fluoro-metil-choline PET/CT | ||||||||||||||||||
Medical condition: patients with prostate cancer istologically proven | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005856-12 | Sponsor Protocol Number: 20221 | Start Date*: 2022-01-31 | |||||||||||
Sponsor Name:Helsinki University Central Hospital | |||||||||||||
Full Title: Monoclonal gammopathies of renal significance (MGRS) in Finland | |||||||||||||
Medical condition: Rare renal diseases linked to monoclonal gammopathy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007742-35 | Sponsor Protocol Number: FINA-003 | Start Date*: 2008-10-01 | |||||||||||
Sponsor Name:MerLion Pharmaceuticals GmbH | |||||||||||||
Full Title: A double-blind, double-dummy, prospective, randomized multiple-site study of oral Finafloxacin 300 mg b.i.d. versus oral Ciprofloxacin 250 mg b.i.d. in patients with lower uncomplicated UTI (uUTI) ... | |||||||||||||
Medical condition: Lower uncomplicated Urinary Tract Infection | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
