- Trials with a EudraCT protocol (620)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
620 result(s) found for: Urinary System.
Displaying page 1 of 31.
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 | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: IT (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 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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 | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
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 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
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 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
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 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Ongoing) | |||||||||||||
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 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003885-40 | Sponsor Protocol Number: ACEARB 1 | Start Date*: 2005-10-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PROVINCIALE DI LECCO | |||||||||||||
Full Title: ACE-inhibitors and Angiotensin two receptor antagonists in IgA nephropathy with mild proteinuria | |||||||||||||
Medical condition: The primary aim of the study consists in testing the hypothesis that blockade of the RAS may decrease the risk of developing adverse effects in patients with benign IgAN.Such blockade would first a... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004411-21 | Sponsor Protocol Number: B109LB1 | Start Date*: 2007-01-04 | |||||||||||
Sponsor Name:Organisation name was not entered | |||||||||||||
Full Title: The effect of aldosterone inhibition on proteinuria in patients with progressive renal disease. | |||||||||||||
Medical condition: Patients with chronic nephropathy and proteinuria over 0,5 g/24 hrs are to be given an inhibitor of aldosterone. Theory tells that aldosterone plays an active role in nephropathy and if that can be... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003045-33 | Sponsor Protocol Number: FENO HSR | Start Date*: 2008-08-25 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: Fenoldopam and renal insufficiency | |||||||||||||
Medical condition: patients undergoing heart surgery developing, in any moment during post surgery hospitalization in Intensive Care Unit, renal problems named as "R" of RIFLE score | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020722-18 | Sponsor Protocol Number: DESMOPRESINA | Start Date*: 2009-04-17 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: 1-DEAMINO 8-D-ARGININA VASOPRESSIN IN PERCUTANEOUS ULTRASOUND-GUIDED RENAL BIOPSY: A RANDOMIZED CONTROLLED TRIAL | |||||||||||||
Medical condition: Patients undergoing percutaneous ultrasound-guided biopsy of native kidney and at high risk of bleeding | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020401-32 | Sponsor Protocol Number: darbepoetina | Start Date*: 2010-01-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: IDENTIFICATION OF OXIDATIVE-STRESS AND MICROINFLAMMATION GENES MODULATED BY ERYTHROPOIETIN ADMINISTRATION IN PATIENTS WITH RENAL TRANSPLANT AND CHRONIC RENAL FAILURE. PERSPECTIVES FOR ERYTHROPOITIN... | |||||||||||||
Medical condition: PATIENTS WITH RENAL TRANSPLANT AND CHRONIC RENAL FAILURE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016762-87 | Sponsor Protocol Number: early transition | Start Date*: 2006-03-24 | |||||||||||
Sponsor Name:OSPEDALE MAGGIORE DI MILANO (IRCCS) | |||||||||||||
Full Title: a randomized, open-label study to evaluate the safety and efficacy of delayed introduction of sirolimus and concomitant tacrolimus elimination in de novo renal allograft recipients | |||||||||||||
Medical condition: no | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000805-23 | Sponsor Protocol Number: LEV102341 | Start Date*: 2004-09-21 | |||||||||||
Sponsor Name:GLAXO SMITHKLINE | |||||||||||||
Full Title: A national, multicentric, randomised, controlled trial. Applications of a critical pathway using LEVOFLOXACIN for the management of patients with abnormal PSA | |||||||||||||
Medical condition: prostatitis | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000451-34 | Sponsor Protocol Number: FARM5XWMZ4 | Start Date*: 2007-10-01 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA DELLA SECONDA UNIVERSITA` DEGLI STUDI DI NAPOLI | |||||||||||||
Full Title: Therapy of hyperhomocysteinemia in hemodialysis patients:effects of acetylcysteine and folates. | |||||||||||||
Medical condition: Hyperhomocysteinemia in hemodialysis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001673-25 | Sponsor Protocol Number: VALSARTAN-TRAPIANTO/04 | Start Date*: 2004-07-30 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: EFFECTS OF ANGIOTENSIN RECEPTOR ANTAGONIST ON CHRONIC NEPHROPATY IN KIDNEY TRANSPLANTED PATIENTS. A PILOT STUDY. | |||||||||||||
Medical condition: CHRONIC NEPHROPATY REDUCTION | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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: 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: 2013-003585-14 | Sponsor Protocol Number: SNOXH94C301 | Start Date*: 2014-01-10 | |||||||||||||||||||||
Sponsor Name:NOXXON Pharma AG | |||||||||||||||||||||||
Full Title: Safety, PK/PD and efficacy of NOX-H94 in dialysis patients with ESA-hyporesponsive anaemia: A randomized, double blind, placebo controlled parallel group study with a single blind cross-over group | |||||||||||||||||||||||
Medical condition: Erythropoiesis stimulating agents (ESA) hyporesponsive anaemia in renal dialysis patients | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) AT (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
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