- Trials with a EudraCT protocol (684)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
684 result(s) found for: Terminal disease.
Displaying page 3 of 35.
EudraCT Number: 2009-011497-15 | Sponsor Protocol Number: CERA | Start Date*: 2009-05-07 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: PILOT CLINICAL TRIAL WITH MIRCERA (methoxy polyethylene glycol-epoetin beta) IN DIALYSIS UNIT OF A.O. SAN GIOVANNI BATTISTA DI TORINO | |||||||||||||
Medical condition: End stage renal patients in hemodialysis or peritoneal dialysis treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018718-57 | Sponsor Protocol Number: REDERT | Start Date*: 2010-06-17 | |||||||||||
Sponsor Name:AZIENDA UNITA` SANITARIA LOCALE N 12 DI VIAREGGIO | |||||||||||||
Full Title: Role of on-line hemodiafiltration (HDF) in the modulation of resistance to erythropoiesis stimulating agents (REDERT) | |||||||||||||
Medical condition: patients on chronic hemodialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001407-11 | Sponsor Protocol Number: Certican MHH PRTx01 | Start Date*: 2006-07-18 | |||||||||||
Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
Full Title: A single center study investigating ciclosporine A microemulsion in combination with basiliximab and prednisolon and switch to low-dose ciclosporine A and everolimus without steroids in the prevent... | |||||||||||||
Medical condition: Kidney transplantation after end stage renal failure | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016801-40 | Sponsor Protocol Number: IP-001-09 | Start Date*: 2016-01-26 | |||||||||||
Sponsor Name:IPERBOREAL PHARMA | |||||||||||||
Full Title: Efficacy and Safety assessments of a peritoneal dialysis solution containing Glucose, Xylitol and L-Carnitine compared to standard PD solutions in Continuous Ambulatory Peritoneal Dialysis (CAPD) | |||||||||||||
Medical condition: Patients with ESRD treated by CAPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002744-24 | Sponsor Protocol Number: 1058/12 | Start Date*: 2012-12-16 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Effect of oral paricalcitol on endothelial function and FGF-23 in peritoneal dialysis patients: a pilot study | |||||||||||||
Medical condition: CHRONIC RENAL FAILURE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002192-35 | Sponsor Protocol Number: 19225 | Start Date*: 2020-10-13 | |||||||||||
Sponsor Name:Bayer - AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multi-center study to assess the efficacy and safety of BAY 2327949 in patients with chronic kidney disease (eGFR range from 25 to 60 mL/min/1.73 m²)... | |||||||||||||
Medical condition: Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) NO (Prematurely Ended) DK (Prematurely Ended) NL (Prematurely Ended) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001710-19 | Sponsor Protocol Number: LUMINALSONAZOID001 | Start Date*: 2022-11-01 |
Sponsor Name:Medical department, Haukeland University Hospital | ||
Full Title: Sonographic diagnostics with oral contrast for Crohns. A novel method for detecting Crohns disease using sonographic intraluminal contrast. | ||
Medical condition: Crohns disease in the terminal ileum | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000304-41 | Sponsor Protocol Number: FG-506E-12-03 | Start Date*: 2004-12-15 | |||||||||||
Sponsor Name:Astellas Pharma GmbH | |||||||||||||
Full Title: A MULTICENTRE, 1:1 RANDOMISED, DOUBLE BLIND, TWO ARM PARALLEL GROUP STUDY TO EVALUATE AND COMPARE THE EFFICACY AND SAFETY OF MODIFIED RELEASE TACROLIMUS FK506E (MR4) VERSUS TACROLIMUS FK506 IN COMB... | |||||||||||||
Medical condition: Patients with end stage kidney disease who will undergo renal transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SE (Completed) HU (Completed) FI (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000421-27 | Sponsor Protocol Number: 21177 | Start Date*: 2022-01-07 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, parallel-group, multicenter Phase 3 study to investigate the efficacy and safety of FInerenone, in addition to standard of care, on the progression o... | |||||||||||||
Medical condition: Non-diabetic chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) CZ (Trial now transitioned) ES (Trial now transitioned) IT (Trial now transitioned) GR (Trial now transitioned) BG (Trial now transitioned) HU (Trial now transitioned) BE (Trial now transitioned) PT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003957-27 | Sponsor Protocol Number: 20115 | Start Date*: 2020-07-15 | |||||||||||||||||||||
Sponsor Name:Bayer AG | |||||||||||||||||||||||
Full Title: A randomized, double-blind, parallel group, placebo-controlled, multi-center study to assess the safety and tolerability of monthly subcutaneous administrations of a low and high dose cohort of oso... | |||||||||||||||||||||||
Medical condition: Prevention of thromboembolic events in ESRD patients on hemodialysis who are at risk for thromboembolic events | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) AT (Completed) GR (Completed) BE (Completed) PT (Completed) NL (Completed) LT (Completed) PL (Completed) HU (Completed) BG (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020872-49 | Sponsor Protocol Number: PI10-Pr.CHOUKROUN-FRENCH | Start Date*: 2013-04-18 | |||||||||||
Sponsor Name:CHU Amiens | |||||||||||||
Full Title: Étude randomisée, en double aveugle, versus placebo, évaluant chez des patients porteurs d'une MRC, non dialysés, l'effet du traitement par carbonate de sevelamer sur le contrôle des taux sériques ... | |||||||||||||
Medical condition: Maladies Rénales Chroniques au stade 3b et 4 (DFG compris entre 15 et 45 ml/min) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003885-16 | Sponsor Protocol Number: SVCARB00606 | Start Date*: 2008-08-19 | |||||||||||
Sponsor Name:Genzyme Europe BV | |||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Sevelamer Carbonate Tablets Dosed Three Times a Day in Hyperphosphatemic Chronic Kidney Disease Patien... | |||||||||||||
Medical condition: Treatment of hyperphosphataemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Prematurely Ended) SE (Prematurely Ended) ES (Completed) AT (Prematurely Ended) IT (Prematurely Ended) HU (Prematurely Ended) DE (Prematurely Ended) GR (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002930-33 | Sponsor Protocol Number: 1366-0022 | Start Date*: 2021-09-02 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH&Co. | |||||||||||||
Full Title: Randomised, double-blind (within dose groups), placebo-controlled and parallel group trial to investigate the effects of different doses of oral BI 685509 given over 20 weeks on UACR reduction in p... | |||||||||||||
Medical condition: non-diabetic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) PT (Completed) DE (Completed) PL (Completed) ES (Restarted) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003297-53 | Sponsor Protocol Number: 18748 | Start Date*: 2020-10-15 | ||||||||||||||||
Sponsor Name:Bayer AG | ||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multi-center study to assess the safety and efficacy of individually titrated oral doses of runcaciguat in subjects with clinical diagnosis of chroni... | ||||||||||||||||||
Medical condition: Treatment of cardiovascular and renal disease in patients with chronic kidney disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) DK (Completed) IT (Completed) FI (Completed) SE (Completed) ES (Completed) PL (Completed) AT (Completed) BE (Completed) BG (Completed) SK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001363-31 | Sponsor Protocol Number: M05-741 | Start Date*: 2007-05-28 | |||||||||||
Sponsor Name:Abbott GmbH & Co KG | |||||||||||||
Full Title: Estudio VITAL- Estudio del activador del receptor de la vitamina D selectivo (Paricalcitol) para la reducción de la albúmina: Estudio multicéntrico de fase II, prospectivo aleatorizado, a doble cie... | |||||||||||||
Medical condition: Nefropatía diabética Tipo 2. Type 2 diabetic nephropathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) PT (Completed) GR (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004789-36 | Sponsor Protocol Number: 173-01 | Start Date*: 2022-06-29 |
Sponsor Name:Universität Heidelberg | ||
Full Title: Randomized, controlled trial of the use of intranasal midazolam for the treatment of terminal agitation in palliative care patients | ||
Medical condition: Terminal agitation in the final phase | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002551-11 | Sponsor Protocol Number: HP-CKDPKD | Start Date*: 2022-01-18 | ||||||||||||||||
Sponsor Name:Aarhus University | ||||||||||||||||||
Full Title: Chronic kidney disease – imaging the metabolic derangements with ultra-sensitive MRI | ||||||||||||||||||
Medical condition: Chronic kidney disease and polycystic kidney disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004099-26 | Sponsor Protocol Number: 6.version,september2011 | Start Date*: 2009-12-10 | ||||||||||||||||
Sponsor Name:Departmnet of nephrology | ||||||||||||||||||
Full Title: Randomised trial on combined effects of dual blockade of the renin angiotensin system and phosphate binding in diabetic and non-diabetic patients with impaired renal function. | ||||||||||||||||||
Medical condition: decreased renal function (CKD II-IV), creatinin clearance 15-90 ml/min | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000654-55 | Sponsor Protocol Number: CVD-001 | Start Date*: 2012-08-01 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: Spironolactone to Prevent Cardiovascular Events in Early Stage Chronic Kidney Disease (CKD): A Pilot Trial | |||||||||||||
Medical condition: chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020404-29 | Sponsor Protocol Number: H9V-MC-GFRF | Start Date*: 2011-04-08 | |||||||||||
Sponsor Name:Eli Lilly and Company Limited, Indianapolis | |||||||||||||
Full Title: A Randomized, Double-Masked, Placebo-Controlled, Multicenter, Phase 2 Study to Evaluate the Safety and Renal Efficacy of LY2382770 in Patients with Diabetic Kidney Disease due to Type 1 or Type 2 D... | |||||||||||||
Medical condition: Patients with Diabetic Kidney Disease due to Type 1 or Type 2 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
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