- Trials with a EudraCT protocol (95)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
95 result(s) found for: Lower urinary tract symptoms.
Displaying page 1 of 5.
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: 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: 2014-001321-32 | Sponsor Protocol Number: 198809 | Start Date*: 2015-04-14 | |||||||||||
Sponsor Name:Department of Clinical Microbiology, Hvidovre Hospital | |||||||||||||
Full Title: The efficacy of pivmecillinam 3 days respectively 5 days t.i.d against community acquired uncomplicated urinary tract infections | |||||||||||||
Medical condition: Lower Uncomplicated Urinary Tract Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006656-35 | Sponsor Protocol Number: A3711047 | Start Date*: 2007-06-12 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: A Multi-center, Randomized, Parallel Group, Double-blind, Placebo Controlled Estimation Study to Assess the Efficacy and Safety of Modified Release UK-369,003 in the Treatment of Men with Storage L... | |||||||||||||
Medical condition: Storage male lower urinary tract symptoms (LUTS) with and without erectile dysfunction (ED). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) FI (Completed) DE (Completed) GB (Completed) GR (Completed) LV (Completed) IT (Completed) SK (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004573-29 | Sponsor Protocol Number: DORI-06 | Start Date*: 2005-01-21 | |||||||||||
Sponsor Name:Peninsula Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Multicenter, Phase 3 Study to Confirm the Safety and Efficacy of Intravenous Doripenem in Complicated Lower Urinary Tract Infection or Pyelonephritis | |||||||||||||
Medical condition: Complicated Lower Urinary Tract Infection or Pyelonephritis MedDRA: Lower urinary tract infection or pyelonephritis (10024981 and/or 10059517) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004380-58 | Sponsor Protocol Number: A3711045 | Start Date*: 2007-03-15 | |||||||||||
Sponsor Name:Pfizer Limited | |||||||||||||
Full Title: A MULTI-CENTER, RANDOMIZED, CROSS-OVER, DOUBLE-BLIND, THIRD PARTY OPEN, PLACEBO CONTROLLED, PILOT STUDY TO ASSESS THE URODYNAMIC EFFECTS OF MODIFIED RELEASE UK-369,003 IN MEN WITH LOWER URINARY TRA... | |||||||||||||
Medical condition: Lower Urinary Tract Symptoms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) CZ (Completed) LV (Prematurely Ended) | |||||||||||||
Trial results: View results |
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 | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004529-99 | Sponsor Protocol Number: CanUTI-7 | Start Date*: 2015-11-17 | |||||||||||
Sponsor Name:Bionorica SE | |||||||||||||
Full Title: A double-blind, controlled, parallel-group, randomized, multicenter clinical trial to assess the efficacy and safety of a herbal drug containing centaury, lovage root, and rosemary leaf (CLR) in co... | |||||||||||||
Medical condition: Acute lower uncomplicated urinary tract infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004378-28 | Sponsor Protocol Number: A3711044 | Start Date*: 2007-06-04 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: A MULTI-CENTER, RANDOMIZED, PARALLEL GROUP, DOUBLE-BLIND, PLACEBO CONTROLLED PROOF OF CONCEPT AND DOSE RANGING STUDY WITH AN ACTIVE CONTROL TO ASSESS THE EFFICACY AND SAFETY/TOLERABILITY OF UK-369,... | |||||||||||||
Medical condition: Lower urinary tract symptoms (LUTS) in men with and without erectile dysfunction (ED). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) FI (Completed) DK (Completed) CZ (Completed) LT (Completed) GB (Completed) GR (Completed) IT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001332-26 | Sponsor Protocol Number: IJG-SCOUT-2021 | Start Date*: 2021-09-06 | |||||||||||
Sponsor Name:IDIAP Jordi Gol | |||||||||||||
Full Title: Clinical effectiveness and bacteriological eradication of 3 short-course antibiotic regimens and single-dose of fosfomicyn trometamol for lower urinary tract infections in adult women [SCOUT study]. | |||||||||||||
Medical condition: Uncomplicated Lower urinary tract infections (uLUTI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002747-14 | Sponsor Protocol Number: OF_FUM_CT1 | Start Date*: 2021-05-24 | |||||||||||
Sponsor Name:"Olainfarm" AS | |||||||||||||
Full Title: A multi-center, randomized, double-blind, double-dummy, parallel-group, active drug controlled, adaptive, Phase III study to investigate efficacy, safety and tolerability of Furamag (Furaginum solu... | |||||||||||||
Medical condition: Microbiologically confirmed acute uncomplicated lower urinary tract infections in women. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003244-13 | Sponsor Protocol Number: D4280C00016 | Start Date*: 2015-04-17 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: A single blind, randomised, multi-centre, active controlled, trial to evaluate safety, tolerability, pharmacokinetics and efficacy of ceftazidime and avibactam compared with cefepime in children fr... | |||||||||||||
Medical condition: Complicated urinary tract infections | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) GR (Completed) PL (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
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: 2015-004013-25 | Sponsor Protocol Number: IMBE-01/2015 | Start Date*: 2016-09-20 | |||||||||||
Sponsor Name:Institute of Molecular Medicine and Biomedical Research- I.M.B.E. | |||||||||||||
Full Title: Mirabegron in the management of lower urinary tract symptoms (LUTS) related to double-J (JJ) ureteral stents. | |||||||||||||
Medical condition: Insertion of a JJ stent, prior to extracorporal shock wave lithotripsy (ESWL) and post ureterolithotripsy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003923-21 | Sponsor Protocol Number: 0826-054 | Start Date*: 2008-12-17 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III, Randomized, Active Comparator-Controlled Clinical Trial to Study the Safety and Efficacy of MK-0826/Ertapenem and Meropenem in Patients with Complicated Urinary Tract Infections | |||||||||||||
Medical condition: Complicated urinary tract infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) ES (Prematurely Ended) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015953-18 | Sponsor Protocol Number: DORIPED3002 | Start Date*: 2010-05-28 | |||||||||||
Sponsor Name:Janssen-Cilag International NV, Turnhoutseweg 30, 2340 Beerse, Belgium | |||||||||||||
Full Title: A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Cefepime in Hospitalized Children With Complicated Urinary Tract Infec... | |||||||||||||
Medical condition: Complicated Urinary Tract Infections | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) CZ (Completed) PL (Temporarily Halted) LV (Prematurely Ended) DE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005117-31 | Sponsor Protocol Number: W-4282-301 | Start Date*: 2018-10-17 | ||||||||||||||||
Sponsor Name:Wockhardt Bio AG | ||||||||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Multicenter, Comparative Study to Determine the Efficacy and Safety of Cefepime-Tazobactam vs. Meropenem followed by Optional Oral Therapy in the Treatment of... | ||||||||||||||||||
Medical condition: Complicated urinary tract infection or acute pyelonephritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Temporarily Halted) BG (Temporarily Halted) LV (Completed) LT (Temporarily Halted) PL (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023452-87 | Sponsor Protocol Number: CXA-cUTI-10-04 | Start Date*: 2011-08-11 | |||||||||||
Sponsor Name:Cubist Pharmaceuticals, Inc. | |||||||||||||
Full Title: A MULTICENTER, DOUBLE-BLIND, RANDOMIZED, PHASE 3 STUDY TO COMPARE THE SAFETY AND EFFICACY OF INTRAVENOUS CXA 201 AND INTRAVENOUS LEVOFLOXACIN IN COMPLICATED URINARY TRACT INFECTION, INCLUDING PYELO... | |||||||||||||
Medical condition: Complicated Urinary Tract Infection, Including Pyelonephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) SK (Completed) LV (Completed) EE (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004422-17 | Sponsor Protocol Number: ANDRO-AOUC-2014-1 | Start Date*: 2015-04-14 | ||||||||||||||||
Sponsor Name:UNIVERSITY OF FLORENCE | ||||||||||||||||||
Full Title: Double-blinded placebo-controlled study on men with lower urinary tract symptoms secondary to prostatic hyperplasia (LUTS-BPH) to assess changes in pressure flow study (PFS) and in molecular profil... | ||||||||||||||||||
Medical condition: lower urinary tract symptoms/benign prostatic hyperplasia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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