- Trials with a EudraCT protocol (473)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
473 result(s) found for: Bladder disease.
Displaying page 3 of 24.
EudraCT Number: 2009-018246-38 | Sponsor Protocol Number: Jun_11_2009_Updated_Nov_2009 | Start Date*: 2010-12-23 | |||||||||||||||||||||
Sponsor Name:Antoni van Leeuwenhoek Ziekenhuis | |||||||||||||||||||||||
Full Title: Phase II trial evaluating combined image guided radiotherapy with Panitumumab (Vectibix®) in patients with muscle invasive transitional cell carcinoma of the bladder | |||||||||||||||||||||||
Medical condition: patients with muscle invasive transitional cell carcinoma of the bladder | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005095-18 | Sponsor Protocol Number: ICR-CTSU/2013/10041 | Start Date*: 2014-09-19 | |||||||||||
Sponsor Name:The Institute of Cancer Research | |||||||||||||
Full Title: A phase II randomised feasibility study of chemoresection and surgical management in low risk non muscle invasive bladder cancer. | |||||||||||||
Medical condition: Low risk non muscle invasive bladder cancer | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003842-18 | Sponsor Protocol Number: A301223 | Start Date*: 2014-04-24 | |||||||||||||||||||||
Sponsor Name:Erasmus MC | |||||||||||||||||||||||
Full Title: Prevention of renal and bladder damage in children with spina bifida by means of early injections with Botulinum-Toxin-A (Botox): a pilot study. | |||||||||||||||||||||||
Medical condition: Neurogenic bladder function disease in spina bifida patients. | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001826-28 | Sponsor Protocol Number: BL-2007-02 | Start Date*: 2007-11-28 | |||||||||||
Sponsor Name:Queen Mary University London | |||||||||||||
Full Title: A phase II/III, randomised, two-arm comparison of maintenance lapatinib versus placebo after firrst-line chemotherapy in patients with HER1 and/or HER2 over expressing locally advanced or metastati... | |||||||||||||
Medical condition: The medical condition being investigated in this trial is locally advanced or metastatic urological cancer. The tumour must overexpress HER1 and/or HER2 gene. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002765-22 | Sponsor Protocol Number: SOGUG-2017-A-IEC(VEJ)-2/NEODURVARIB | Start Date*: 2018-09-04 | |||||||||||
Sponsor Name:Spanish Oncology Genitourinary Group - SOGUG | |||||||||||||
Full Title: Impact of the combination of durvalumab (MEDI4736) plus olaparib (AZD2281) administered prior to surgery in the molecular profile of resectable urothelial bladder cancer | |||||||||||||
Medical condition: Resectable urothelial bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000192-42 | Sponsor Protocol Number: 191622-516 | Start Date*: 2007-07-25 | |||||||||||
Sponsor Name:Allergan Ltd | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study of the Safety and Efficacy of a Single Treatment with Two Dose Levels of BOTOX® (Botulinum Toxin Type A) Purified N... | |||||||||||||
Medical condition: Urinary incontinence due to neurogenic detrusor overactivity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) NL (Completed) PT (Completed) ES (Completed) IT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007053-13 | Sponsor Protocol Number: STEG-CORP_111802 | Start Date*: 2009-07-31 | |||||||||||
Sponsor Name:Grachtenhaus-Apotheke, Inh. Klaus Stegemann e. K. | |||||||||||||
Full Title: Doppelblinde, randomisierte, Placebo-kontrollierte Studie der Phase III zur Bestimmung der Wirksamkeit, Verträglichkeit und Sicherheit von intravesikal verabreichter Oxybutynin-Lösung bei Kindern/J... | |||||||||||||
Medical condition: bladder disorder (detrusor hyperactivity caused by neurogenic disorder) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001823-38 | Sponsor Protocol Number: AB65/18 | Start Date*: 2018-11-26 | |||||||||||
Sponsor Name:Technische Universität München, Fakultät für Medizin vertreten durch den Dekan | |||||||||||||
Full Title: A prospective, single arm, multicenter, phase II-trial to assess safety and efficacy of preoperative RAdiation therapy before radical CystEctomy combined with ImmunoTherapy in locally advanced urot... | |||||||||||||
Medical condition: Locally advanced urothelial bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002676-40 | Sponsor Protocol Number: CA045-009 | Start Date*: 2019-07-03 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3, Randomized, Study of Neoadjuvant and Adjuvant Nivolumab Plus Bempegaldesleukin (NKTR-214), Versus Nivolumab Alone Versus Standard of Care in Participants with Muscle-Invasive Bladder Can... | |||||||||||||
Medical condition: Muscle-Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) AT (Completed) GR (Completed) ES (Ongoing) CZ (Completed) PL (Completed) FR (Completed) BE (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002100-13 | Sponsor Protocol Number: ESR-16-12611 | Start Date*: 2018-10-11 | |||||||||||
Sponsor Name:Hellenic GenitoUrinaty Cancer Group (HGUCG) | |||||||||||||
Full Title: Intravesical administration of Durvalumab (MEDI4736) to patients with high-risk, non-muscle-invasive bladder cancer (NMIBC). A phase II study with correlative biomarker studies. | |||||||||||||
Medical condition: Non-muscle-invasive bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002826-55 | Sponsor Protocol Number: SECAVIN-12 | Start Date*: 2012-10-17 | ||||||||||||||||
Sponsor Name:Associació Per a la Recerca Oncològica (APRO) | ||||||||||||||||||
Full Title: A randomised Phase II/III study of cabazitaxel versus vinflunine in metastatic or locally advanced transitional cell carcinoma of the urothelium | ||||||||||||||||||
Medical condition: metastatic or locally advanced transitional cell carcinoma of the urothelium | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003813-92 | Sponsor Protocol Number: EPT02/2016 | Start Date*: 2017-01-25 | |||||||||||
Sponsor Name:IBSA FARMACEUTICI ITALIA SRL | |||||||||||||
Full Title: Open clinical trial to evaluate the efficacy of intravesical instillation of hyaluronate added to early instillation of mitomycin vs early instillation of mitomycin in patients suffering from low r... | |||||||||||||
Medical condition: Low risk not muscle-infiltrating bladder neoplasia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001268-57 | Sponsor Protocol Number: 905-CL-058 | Start Date*: 2007-09-12 | ||||||||||||||||
Sponsor Name:Astellas Pharma US, Inc. | ||||||||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Parallel Group, Placebo Controlled, Multi-Center Study to Evaluate the Safety of the Co-administration of Solifenacin Succinate with 0.4 mg Tamsulosin Hydrochlo... | ||||||||||||||||||
Medical condition: Storage and Voiding Lower Urinary Tract Symptoms (LUTS) and Bladder Outlet Obstruction (BOO) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: CZ (Completed) BE (Completed) HU (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021265-80 | Sponsor Protocol Number: PHRCNATHorsCancer2010-HC11-05 | Start Date*: 2010-10-18 | |||||||||||
Sponsor Name:Centre Hospitalier Universitaire de Reims | |||||||||||||
Full Title: Injections intradétrusoriennes de toxine botulique A chez l'enfant présentant un syndrome d'hyperactivité vésicale neurogène : essai thérapeutique contrôlé multicentrique de non infériorité entre d... | |||||||||||||
Medical condition: Syndrome d'hyperactivité vésicale neurogène chez l'enfant | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
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: 2010-023406-13 | Sponsor Protocol Number: DZITM1 | Start Date*: 2011-03-18 | |||||||||||
Sponsor Name:Städtische Kliniken Neuss, Lukaskrankenhaus GmbH | |||||||||||||
Full Title: Target-spezifische Therapie mit Pazopanib zusätzlich zu Vinflunin bei Patienten mit fortgeschrittenem oder metastasiertem Urothelkarzinom nach Versagen einer platinhaltigen Therapie | |||||||||||||
Medical condition: Advanced urothelial carcinoma of the bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006935-38 | Sponsor Protocol Number: A0221008 | Start Date*: 2007-04-16 | |||||||||||
Sponsor Name:Pfizer Inc. NYO-685-21-14,685 3rd Avenue, NEW YORK, NY 10017. US | |||||||||||||
Full Title: 12-WEEK, RANDOMIZED, DOUBLE-BLIND, DOUBLE-DUMMY, PLACEBO-CONTROLLED, PARALLEL-GROUP, MULTICENTER TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF FESOTERODINE IN COMPARISON TO TOLTERODINE ER IN PATIENT... | |||||||||||||
Medical condition: Treatment of overactive bladder with symptoms of frequency, urgency, and urgency incontinence. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) ES (Completed) BE (Completed) HU (Completed) DK (Completed) CZ (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004844-27 | Sponsor Protocol Number: SURE-01 | Start Date*: 2021-06-01 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: SURE-01_An open label, single-arm, phase 2 study of neoadjuvant sacituzumab govitecan, before radical cystectomy, for patients with muscle-invasive bladder cancer who cannot receive or refuse cispl... | |||||||||||||
Medical condition: Muscle-invasive bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002361-39 | Sponsor Protocol Number: BAY 79-4998 / 12331 | Start Date*: 2006-12-01 | |||||||||||
Sponsor Name:Bayer Vital GmbH | |||||||||||||
Full Title: A 4-week, open-label, multicenter, urodynamic pilot study to explore the efficacy, tolerability and safety of darifenacin (7.5 mg with up-titration to 15 mg) in patients with multiple sclerosis and... | |||||||||||||
Medical condition: Neurogenic overactive bladder disaese in patients with multiple sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000905-19 | Sponsor Protocol Number: Rec0/0438-IT-CL0491 | Start Date*: 2018-01-29 | |||||||||||
Sponsor Name:Recordati S.p.A | |||||||||||||
Full Title: EFFECTS OF TWO DIFFERENT DOSES OF REC 0/0438 ADMINISTERED BY INTRA-VESICAL INSTILLATION IN PATIENTS WITH NEUROGENIC DETRUSOR OVERACTIVITY DUE TO SPINAL CORD INJURY: A REPEATED DOSES, DOUBLE-BLIND,... | |||||||||||||
Medical condition: neurogenic detrusor overactivity due to spinal cord injury | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) PL (Completed) CZ (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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