- Trials with a EudraCT protocol (24)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
24 result(s) found for: Cystitis AND Urinary Tract Infection.
Displaying page 1 of 2.
EudraCT Number: 2013-003327-11 | Sponsor Protocol Number: 3623 | Start Date*: 2015-02-10 | |||||||||||
Sponsor Name:University of Southampton | |||||||||||||
Full Title: Alternative Treatments of Adult female Urinary Tract Infection: a double blind, placebo controlled,factorial randomised trial of Uva ursi and open pragmatic trial of ibuprofen. | |||||||||||||
Medical condition: Acute urinary tract infections. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005706-11 | Sponsor Protocol Number: Cyst2016_01 | Start Date*: 2016-03-14 | |||||||||||
Sponsor Name:Vita Green Europa S.A. | |||||||||||||
Full Title: Single-site, open, randomized clinical trial to assess the non-inferiority of Cysticlean® versus Fosfomicina in the treatment of cystitis in women in Spain. | |||||||||||||
Medical condition: Urinary Tract Infection (UTI) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001448-78 | Sponsor Protocol Number: Cyst2018_01 | Start Date*: 2018-11-08 | |||||||||||
Sponsor Name:Vita Green Europa S.A. | |||||||||||||
Full Title: Single-site, open, randomized clinical trial to assess the non-inferiority of Cysticlean® versus Fosfomicina in the treatment of cystitis in women in Spain. | |||||||||||||
Medical condition: Urinary Tract Infection (UTI) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003367-23 | Sponsor Protocol Number: 672-CL-035 | Start Date*: 2006-02-13 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study of YM672 in the Treatment of Painful Bladder Syndrome/Interstitial Cystitis | |||||||||||||
Medical condition: Interstitial Cystitis / Painful Bladder Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000553-27 | Sponsor Protocol Number: 212390 | Start Date*: 2020-06-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A Phase III, Randomized, Multicenter, Parallel-Group, Double-Blind, Double-Dummy Study in Adolescent and Adult Female Participants Comparing the Efficacy and Safety of Gepotidacin to Nitrofurantoin... | |||||||||||||
Medical condition: Urinary Tract Infection (Acute Cystitis) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002776-14 | Sponsor Protocol Number: 97 | Start Date*: 2013-03-15 | |||||||||||
Sponsor Name:University of Oslo, Faculty of medicine, Institute of Health and Society | |||||||||||||
Full Title: Ibuprofen versus mecillinam for uncomplicated cystitis in adult, non-pregnant women | |||||||||||||
Medical condition: Uncomplicated cystitis in adult, non pregnant women, age 18-60. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NO (Completed) DK (Completed) SE (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: 2018-001801-98 | Sponsor Protocol Number: 204989 | Start Date*: 2020-02-27 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A Phase III, Randomized, Multicenter, Parallel-Group, Double-Blind, Double-Dummy Study in Adolescent and Adult Female Participants Comparing the Efficacy and Safety of Gepotidacin to Nitrofurantoin... | |||||||||||||
Medical condition: Urinary Tract Infection (Acute Cystitis) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) BG (Completed) GR (Completed) HU (Completed) CZ (Completed) SK (Completed) RO (Ongoing) | |||||||||||||
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 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
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) | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: PL (Completed) HU (Completed) DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001486-21 | Sponsor Protocol Number: 276046 | Start Date*: 2021-11-26 | |||||||||||
Sponsor Name:University of Helsinki/CLUE working Group | |||||||||||||
Full Title: A Multicentre Randomised Control Trial Assessing the Efficacy of Antimicrobial Prophylaxis for Extracorporeal Shock Wave Lithotripsy on reducing Urinary Tract Infections | |||||||||||||
Medical condition: Nephrolithiasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
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 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000938-19 | Sponsor Protocol Number: 4PH/2012/002 | Start Date*: 2012-06-11 | |||||||||||
Sponsor Name:NOVINTETHICAL PHARMA SAGL | |||||||||||||
Full Title: Safety and Efficacy of tablets containing extract of Hibiscus Sabdariffa (HS) and Propoli versus placebo in the treatment of the cystitis with Ciproxin | |||||||||||||
Medical condition: patients with diagnosys of cystitis confirmed by urine culture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (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) | ||||||||||||||||||||||||||||
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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: 2021-003466-12 | Sponsor Protocol Number: MCMK0220 | Start Date*: 2022-03-25 | |||||||||||
Sponsor Name:MCM Klosterfrau Vertriebsgesellschaft mbH | |||||||||||||
Full Title: A double-blind, randomised, multi-centre, controlled clinical trial to compare D-mannose versus antibiotic in the treatment of acute uncomplicated lower urinary tract infections in female patients | |||||||||||||
Medical condition: acute uncomplicated lower urinary tract infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003857-26 | Sponsor Protocol Number: BIRT | Start Date*: 2013-12-11 |
Sponsor Name:ULB ERASME HOSPITAL | ||
Full Title: The Bacteriuria In Renal Transplantation study: A prospective, randomized, multicenter trial comparing antibiotics versus no treatment in the prevention of urinary tract infection in kidney transpl... | ||
Medical condition: Asymptomatic bacteriuria after renal transplantation. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000906-36 | Sponsor Protocol Number: GEB-IAL-2014-01 | Start Date*: 2014-12-09 |
Sponsor Name:Laboratorios Gebro Pharma S.A. | ||
Full Title: Randomized, parallel, multicenter, phase IV clinical trial to assess the efficacy of hyaluronic acid/chondroitin sulfate versus fosfomycin trometamol in recurrent urinary tract infection prevention. | ||
Medical condition: Recurrent urinary tract infections | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004174-10 | Sponsor Protocol Number: P1351 | Start Date*: 2013-11-18 |
Sponsor Name:UMC St Radboud | ||
Full Title: Pharmacokinetics of nitrofurantoin in the elderly | ||
Medical condition: Uncomplicated urinary tract infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002235-15 | Sponsor Protocol Number: 999975814 | Start Date*: 2020-01-22 |
Sponsor Name:University of Oslo | ||
Full Title: The effect of methenamine hippurate to reduce antibiotic prescribing due to new episodes of urinary tract infections (UTI) in elderly women with recurrent UTI – a triple-blinded,randomized placebo-... | ||
Medical condition: recurrent urinary tract infection in women | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: SE (Completed) NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001838-17 | Sponsor Protocol Number: MV140-SLG-003 | Start Date*: 2015-07-17 | |||||||||||
Sponsor Name:Inmunotek, S.L. [...] | |||||||||||||
Full Title: PROSPECTIVE MULTICENTER CLINICAL TRIAL RANDOMIZED, DOUBLE-BLIND, PARALLEL-CONTROLLED VERSUS PLACEBO IN A POLYVALENT SUBLINGUAL BACTERIAL VACCINE (IN ORAL MUCOSA) TO THREE MONTHS AND SIX MONTHS IN ... | |||||||||||||
Medical condition: Recurrent Urinary Tract Infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
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