- Trials with a EudraCT protocol (466)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
466 result(s) found for: Bladder Disease.
Displaying page 1 of 24.
EudraCT Number: 2006-004465-33 | Sponsor Protocol Number: Cox052006 | Start Date*: 2006-12-04 | |||||||||||
Sponsor Name:Eero Kaasinen | |||||||||||||
Full Title: Oral Celecoxib combined with BCG instillation therapy in treatment of carcinoma in situ (CIS), TaG3 and T1 disease of urinary bladder | |||||||||||||
Medical condition: invasive bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005431-15 | Sponsor Protocol Number: ML 5220 | Start Date*: 2008-12-24 | |||||||||||||||||||||
Sponsor Name:ACHG-K.U.Leuven | |||||||||||||||||||||||
Full Title: PHASE III RANDOMIZED CHEMOPREVENTION STUDY OF SELENIUM ON THE RECURRENCE OF NON-INVASIVE BLADDER CANCER | |||||||||||||||||||||||
Medical condition: Bladder cancer | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002760-16 | Sponsor Protocol Number: 04/QO603/42 HEXVIX | Start Date*: 2005-01-12 | |||||||||||
Sponsor Name:Guy's and St Thomas' NHS Foundation Trust | |||||||||||||
Full Title: A randomised Study of “bluelight” hexyl amino levulinic acid (HAL) photodynamic assisted resection of bladder tumours versus conventional “white light” transurethral resection of newly diagnosed bl... | |||||||||||||
Medical condition: Superficial Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005040-20 | Sponsor Protocol Number: 2012-520 | Start Date*: 2013-01-09 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Effect of Macrodex versus lactated Ringer on coagulation in major surgery. A randomised clincal trial. | |||||||||||||
Medical condition: Neoplasma malignum vesicae urinaria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000687-89 | Sponsor Protocol Number: ICR-CTSU/2008/10018 | Start Date*: 2006-11-20 | |||||||||||
Sponsor Name:Institute of Cancer Research | |||||||||||||
Full Title: A randomised phase III placebo-controlled trial evaluating the addition of celecoxib to standard treatment of transitional cell carcinoma of the bladder | |||||||||||||
Medical condition: Non-muscle Invasive Transitional cell Carcinoma of the Bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003898-98 | Sponsor Protocol Number: PDD_vs_WL-TURB_in_pazienti_con_NMIB | Start Date*: 2013-11-28 | |||||||||||
Sponsor Name:Ospedale San Raffaele | |||||||||||||
Full Title: COMPARISON OF WHITE LIGHT TUR VS PHOTODYNAMIC DIAGNOSIS (PDD)- GUIDED TUR AS ASSESSED BY SECOND LOOK TUR FOR THE TREATMENT OF HIGH RISK NON MUSCLE INVASIVE BLADDER CANCER (NMIBC) | |||||||||||||
Medical condition: high grade non muscle invasive bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000150-22 | Sponsor Protocol Number: T14/2018 | Start Date*: 2018-06-05 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Intravesical instillation therapy with bacillus Calmette-Guérin (BCG) and sequential BCG and electromotive Mitomycin-C (EMDA-MCC) in patients with high risk non-muscle-invasive bladder carcinoma | |||||||||||||
Medical condition: Non-muscle invasive bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003622-18 | Sponsor Protocol Number: TS-004 | Start Date*: 2007-10-01 | |||||||||||
Sponsor Name:State University Hospital | |||||||||||||
Full Title: Efficacy and safety of TachoSil in patients undergoing cystectomy. A pilot study. | |||||||||||||
Medical condition: The trial will evaluate the efficacy and safety of TachoSil in patients undergoing cystectomy for bladder cancer and non-malignant bladder disease. TachoSil will be applied to the anastomoses betwe... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003517-42 | Sponsor Protocol Number: SPI-1012 | Start Date*: 2011-11-23 | |||||||||||||||||||||
Sponsor Name:Spectrum Pharmaceuticals, Inc | |||||||||||||||||||||||
Full Title: A Phase 3 International, Multicenter, Double-Blind, Placebo-Controlled, Randomized Trial Evaluating the Efficacy and Safety of Multiple Instillations of Intravesical Apaziquone vs. Placebo in Patie... | |||||||||||||||||||||||
Medical condition: The medical condition under investigation is noninvasive bladder cancer in patients undergoing transurethral resection of bladder tumor/tumors. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SK (Completed) CZ (Prematurely Ended) ES (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015404-26 | Sponsor Protocol Number: SPI-611 | Start Date*: 2009-11-12 | |||||||||||||||||||||
Sponsor Name:Spectrum Pharmaceuticals, Inc. | |||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Placebo-Controlled, Double-Blind Phase 3 Trial of Single-Dose Intravesical EOquinâ as a Surgical Adjuvant Instilled in the Early Postoperative Period in Patients Undergoi... | |||||||||||||||||||||||
Medical condition: The medical condition under investigation is noninvasive bladder cancer in patients undergoing transurethral resection of bladder tumor. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001811-59 | Sponsor Protocol Number: D933RC00001 | Start Date*: 2019-02-26 | ||||||||||||||||
Sponsor Name:AstraZeneca AB | ||||||||||||||||||
Full Title: A Phase III, Randomized, Open-Label, Multi-Center, Global Study to Determine the Efficacy and Safety of Durvalumab in Combination with Gemcitabine+Cisplatin for Neoadjuvant Treatment Followed by Du... | ||||||||||||||||||
Medical condition: Patients with histologically or cytologically documented muscle-invasive transitional cell carcinoma (TCC) of the bladder | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) NL (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004995-20 | Sponsor Protocol Number: 05/SUR/3360E | Start Date*: 2006-06-08 | |||||||||||
Sponsor Name:R and D Department, Cardiff and the Vale NHS Trust | |||||||||||||
Full Title: A Prospective, Single-Arm, Open-label Study to Investigate the Efficacy and Safety of Intravesical Injection of Botulinum Toxin Type-A (500 Units Dysport®) for the Management of Idiopathic Overacti... | |||||||||||||
Medical condition: Idiopathic Overactive bladder syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004641-27 | Sponsor Protocol Number: UZLeuven | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:UZLeuven | |||||||||||||
Full Title: BOTOX in the treatment of urinary incontinence due to neurogenic detrusor overactivity in patients 3 months - 17 years | |||||||||||||
Medical condition: Urinary incontinence due to neurogenic detrusor overactivity | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003541-11 | Sponsor Protocol Number: BL006 | Start Date*: 2021-04-15 | |||||||||||
Sponsor Name:UroGen Pharma Ltd. | |||||||||||||
Full Title: A Randomized, Controlled, Open-label Study of the Efficacy, Durability, and Safety of UGN-102 With or Without TURBT in Patients with Low Grade Intermediate Risk Non-Muscle Invasive Bladder Cancer (... | |||||||||||||
Medical condition: Non-Muscle Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) BG (Completed) LV (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005274-22 | Sponsor Protocol Number: 1408P1921 | Start Date*: 2014-07-30 | |||||||||||
Sponsor Name:Shionogi & Co., Ltd | |||||||||||||
Full Title: A multicenter, open-label, phase 2 study of S-588410 as maintenance monotherapy after first-line platinum-containing chemotherapy in patients with advanced and/or metastatic bladder cancer | |||||||||||||
Medical condition: Advanced and/or metastatic bladder cancer, which is under control according to first-line chemotherapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005452-38 | Sponsor Protocol Number: D910PC00001 | Start Date*: 2022-07-28 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase III Randomized, Open-Label, Multicenter Study to Determine the Efficacy and Safety of Durvalumab in Combination With Tremelimumab and Enfortumab Vedotin or Durvalumab in Combination With En... | |||||||||||||
Medical condition: Documented muscle-invasive urothelial carcinoma (UC) of the bladder in cisplatin ineligible patients or Who Refuse Cisplatin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) ES (Ongoing) PT (Ongoing) AT (Ongoing) PL (Ongoing) NL (Ongoing) IT (Restarted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002267-33 | Sponsor Protocol Number: OCTO-089 | Start Date*: 2017-06-13 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: A parallel group phase I/II marker lesion study to assess the safety, tolerability and efficacy of intravenous or intravesical pembrolizumab in intermediate risk recurrent non-muscle invasive bladd... | |||||||||||||
Medical condition: Intermediate risk recurrent non-muscle invasive bladder cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004423-11 | Sponsor Protocol Number: 527.66 | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: An uncontrolled, open-label, titration, long-term safety (up to 12 months) and efficacy study of tamsulosin hydrochloride in children with neuropathic bladder, with a randomized pharmacokinetic sub... | |||||||||||||
Medical condition: Neurogenic Bladder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Prematurely Ended) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004996-40 | Sponsor Protocol Number: 04/SUR/3070 | Start Date*: 2006-06-08 | |||||||||||
Sponsor Name:R and D Department, Cardiff and the Vale NHS Trust | |||||||||||||
Full Title: A Prospective, Single-Arm, Open-label Study to Investigate the Efficacy and Safety of Intravesical Injection of Botulinum Toxin Type-A (750 Units Dysport®) for the Management of Neurogenic Detrusor... | |||||||||||||
Medical condition: Neurogenic detrusor overactivity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001321-14 | Sponsor Protocol Number: INCB54828-201 | Start Date*: 2017-01-12 | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 2, Open-Label, Single-Agent, Multicenter Study to Evaluate the Efficacy and Safety of INCB054828 in Subjects With Metastatic or Surgically Unresectable Urothelial Carcinoma Harboring FGF/FG... | |||||||||||||
Medical condition: Subjects with metastatic or surgically unresectable urothelial cancer (may include primary site from ureters, upper tract, renal pelvis, and bladder) with an FGF/FGFR alteration, who failed at leas... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) FR (Completed) ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
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