- Trials with a EudraCT protocol (6,619)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (269)
6,619 result(s) found for: Renal.
Displaying page 15 of 331.
EudraCT Number: 2011-002833-20 | Sponsor Protocol Number: EP-TSC-663 | Start Date*: 2012-08-20 | ||||||||||||||||
Sponsor Name:Oxford University Hospitals NHS Trust | ||||||||||||||||||
Full Title: Prospective study of 18F-RGD PET-CT in assessment of response to antiangiogenic treatment in patients with renal cancer and comparison with perfusion CT | ||||||||||||||||||
Medical condition: Primary and metastatic cancer. The active substance is a diagnostic agent that identifies angiogenesis associated with tumour growth. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-000380-26 | Sponsor Protocol Number: CERTES02 (Ce-PoP-RAD001A2419) | Start Date*: 2005-05-24 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A. | |||||||||||||
Full Title: A 12 month, multicenter, randomized, parallel, open-label study, to evaluate renal function and efficacy of Certican® (everolimus) with Simulect® (basiliximab) and cyclosporine discontinuation at 3... | |||||||||||||
Medical condition: Renal Transplant | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003114-34 | Sponsor Protocol Number: CUR001 | Start Date*: 2007-11-29 |
Sponsor Name:Department of Nephrology and Renal Transplantation, University Hospitals Leuven | ||
Full Title: The impact of oral curcumin (Curcuma longa) on mycophenolic acid and metabolite pharmacokinetics in stable renal allograft recipients: exploratory investigation of the role of intestinal uridine-di... | ||
Medical condition: Stable renal allograft recipients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-015987-32 | Sponsor Protocol Number: AV-951-09-902 | Start Date*: 2010-04-02 | |||||||||||
Sponsor Name:AVEO Pharmaceuticals, Inc. | |||||||||||||
Full Title: An Extension Treatment Protocol for Subjects who have Participated in a Phase 3 Study of Tivozanib vs. Sorafenib in Renal Cell Carcinoma (Protocol AV-951-09-301) | |||||||||||||
Medical condition: Advanced Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Completed) CZ (Completed) HU (Completed) PL (Completed) BG (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000088-40 | Sponsor Protocol Number: 07 300 02 | Start Date*: 2008-04-09 | |||||||||||||||||||||
Sponsor Name:CHU de TOULOUSE | |||||||||||||||||||||||
Full Title: Pharmacocinétique de l’association pipéracilline-tazobactam chez les patients septiques, en insuffisance rénale oligo-anurique, traités par hémodiafiltration veino-veineuse continue | |||||||||||||||||||||||
Medical condition: patient septique hospitalisé en réanimation présentant une infection, déjà colonisé ou non, de localisation variable, à germe non identifié supposé sensible à l’association pipéracilline-tazobactam. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000127-32 | Sponsor Protocol Number: ROPETAR | Start Date*: 2011-11-03 | |||||||||||||||||||||
Sponsor Name:Werkgroep Immunotherapie Nederland voor Oncologie | |||||||||||||||||||||||
Full Title: A randomized phase II study to explore the efficacy and feasibility of upfront bi-monthly rotations between Everolimus and Pazopanib with sequential treatment of first line Pazopanib and second lin... | |||||||||||||||||||||||
Medical condition: Advanced or metastatic clear cell renal cancer. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-000517-36 | Sponsor Protocol Number: CRAD001H2401 | Start Date*: 2005-09-21 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: RESCUE Study (Certican in Liver Transplant Recipients with Renal Insufficiency) A 6-month, multicenter, randomized, open-label study of safety and efficacy of Certican-based regimen versus CNI-b... | ||
Medical condition: maintenance of liver transplant | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) BE (Completed) ES (Completed) IT (Completed) FI (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004606-97 | Sponsor Protocol Number: PMR-EC-1209 | Start Date*: 2007-02-22 | |||||||||||
Sponsor Name:Astellas Pharma GmbH | |||||||||||||
Full Title: A MULTICENTER, SINGLE-ARM, OPEN, CONVERSION STUDY FROM A CYCLOSPORINE (CyA) BASED IMMUNOSUPPRESSIVE REGIMEN TO A TACROLIMUS MODFIED RELEASE, FK506E (MR4), BASED IMMUNOSUPPRESSIVE REGIMEN IN KIDNEY ... | |||||||||||||
Medical condition: Stable, adult kidney transplant recipients (at least 12 months post transplant) who are currently treated with cyclosporine and who meet the Inclusion and Exclusion Criteria will be enrolled. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) DE (Completed) ES (Completed) CZ (Completed) HU (Completed) FI (Completed) SE (Completed) DK (Completed) AT (Completed) PT (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003793-26 | Sponsor Protocol Number: 3066K1-3311-WW | Start Date*: 2008-05-19 | |||||||||||
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | |||||||||||||
Full Title: Phase 3b, Randomized, Open-Label Study of Bevacizumab + Temsirolimus vs. Bevacizumab + Interferon-Alfa as First-Line Treatment in Subjects With Advanced Renal Cell Carcinoma | |||||||||||||
Medical condition: First-Line Treatment in Subjects with Advanced Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) FR (Completed) BE (Completed) PT (Completed) CZ (Completed) DE (Completed) SK (Completed) NL (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004073-76 | Sponsor Protocol Number: CAAA001A12401 | Start Date*: 2020-10-12 | ||||||||||||||||
Sponsor Name:Advanced Accelerator Applications International SA | ||||||||||||||||||
Full Title: A multicenter, open-label post authorization safety study to evaluate the effect of LysaKare® infusion on serum potassium levels in GEP-NET patients eligible for Lutathera® treatment | ||||||||||||||||||
Medical condition: LysaKare® is indicated for reduction of renal radiation exposure during peptide-receptor radionuclide therapy (PRRT) with lutetium (177 Lu) oxodotreotide in adults. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) IT (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000796-32 | Sponsor Protocol Number: 185/13 | Start Date*: 2014-01-28 | |||||||||||
Sponsor Name:Policlinico A. Gemelli | |||||||||||||
Full Title: A multiple centre, randomised, open label, prospective clinical study to compare the efficacy and safety of a combination of tacrolimus with everolimus versus the combination of tacrolimus with MM... | |||||||||||||
Medical condition: KIDNEY TRANSPLANTATION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004947-23 | Sponsor Protocol Number: none | Start Date*: 2006-02-22 |
Sponsor Name:UF de méthodologie en recherche clinique | ||
Full Title: Efficacité de la rapamycine dans la prévention secondaire des cancers cutanés chez les transplantés rénaux. Etude ouverte randomisée Rapamycine vs anticalcineurines | ||
Medical condition: To evaluate the impact of two imnosupressive regimens on the incidence of skin cancers among patients who has a first spinocellular skin cancer after renal transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003589-25 | Sponsor Protocol Number: Levo-AKI | Start Date*: 2014-11-11 |
Sponsor Name:Sahlgrenska Universitetssjukhuset/Sahlgrenska | ||
Full Title: The effect of levosimendan, on renal blood flow, function and oxygen uptake during acute renal failure after cardiac surgery | ||
Medical condition: Acute kidney injury postoperatively in connection with heart surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005867-33 | Sponsor Protocol Number: 13701 | Start Date*: 2009-03-10 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Prospective non-randomized (pharmacoepidemiologic) cohort study (open-label, multicenter) to assess the magnitude of potential risk with the administration of Primovist/Eovist in patients with mode... | |||||||||||||
Medical condition: Patients with moderate (eGFR 30 – 59 mL/min/1.73 m2) to severe renal impairment (eGFR < 30 mL/min/1.73 m2) scheduled to undergo contrast-enhanced MRI with Primovist/Eovist. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002539-27 | Sponsor Protocol Number: IntraRenalTac | Start Date*: 2019-09-23 | |||||||||||
Sponsor Name:Oslo University Hospital – Rikshospitalet | |||||||||||||
Full Title: Association between intrarenal tacrolimus concentration and development of renal interstitial fibrosis in renal transplant recipients | |||||||||||||
Medical condition: Development of renal interstitial fibrosis in renal transplant recipients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000416-91 | Sponsor Protocol Number: CA186001 | Start Date*: 2007-07-20 | |||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||
Full Title: A Phase I/II, Ascending, Multi-Dose Study of BMS-663513, An Agonistic Anti-CD137 Monoclonal Antibody, Administered Every Three Weeks to Patients with Metastatic or Locally Advanced Solid Malignanci... | |||||||||||||||||||||||
Medical condition: Patients with Metastatic or Locally Advanced Solid Malignancies | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-002455-33 | Sponsor Protocol Number: D8480C00030 | Start Date*: 2006-11-13 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II, Randomised, Double-blind, Parallel Group Study to Assess the Efficacy of AZD2171 45mg Versus Placebo following 12 Weeks of Treatment in Patients with Metastatic or Recurrent Renal Cell ... | |||||||||||||
Medical condition: Renal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005403-17 | Sponsor Protocol Number: KH-MS-JAW-01 | Start Date*: 2007-12-10 | ||||||||||||||||
Sponsor Name:GE Healthcare | ||||||||||||||||||
Full Title: A prospective, comparative single center study of Hexvix® fluorescence uretero-renoscopy and white light uretero-renoscopy in the detection of upper urinary tract urothelial cell carcinoma | ||||||||||||||||||
Medical condition: Upper urinary tract (ureters and pyela/renal pelvises) urothelial cell carcinoma for which blue light uretero-renoscopy and biopsies are performed for diagnosis. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003298-24 | Sponsor Protocol Number: EVITAESTEROIDE-12 | Start Date*: 2014-06-26 | |||||||||||
Sponsor Name:Sociedad Andaluza de Trasplante de Órganos y Tejidos (SATOT) | |||||||||||||
Full Title: Steroid withdrawal and novo donor-specific anti-HLA antibodies in renal transplant patients: a prospective, randomized and controlled study in parallel groups. | |||||||||||||
Medical condition: Kidney transplantaion | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002556-41 | Sponsor Protocol Number: TRX 1.0 | Start Date*: 2008-02-07 | |||||||||||
Sponsor Name:Trimed Biotech GmbH | |||||||||||||
Full Title: A randomized, open-label, 2-arm, multicentre, Phase II study to evaluate the safety and efficacy of Trivax, a dendritic cell-based interleukin-12 secreting autologous cancer vaccine, in combination... | |||||||||||||
Medical condition: Metastatic renal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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