- Trials with a EudraCT protocol (61)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
61 result(s) found for: Chronic Kidney Disease (CKD) Hemodialysis.
Displaying page 1 of 4.
EudraCT Number: 2021-000995-13 | Sponsor Protocol Number: DECODE-CKD | Start Date*: 2022-01-26 | |||||||||||
Sponsor Name:Department of Cardiology, Herlev and Gentofte hospital | |||||||||||||
Full Title: A 6-Month, Randomized, Double-Blind Study to Evaluate the Effect of Dapagliflozin on EChOcardiographic Measures of CarDiac StructurE and Function in Patients with Chronic Kidney Disease (DECODE-CKD) | |||||||||||||
Medical condition: Chronic 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: 2010-022994-32 | Sponsor Protocol Number: 34009 | Start Date*: 2011-06-24 | ||||||||||||||||
Sponsor Name:UMC Utrecht | ||||||||||||||||||
Full Title: Effect of N-acetylcysteine on hydrogen sulfide in chronic kidney disease | ||||||||||||||||||
Medical condition: Chronic kidney disease End stage renal disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001520-18 | Sponsor Protocol Number: NL76839.042.21 | Start Date*: 2021-04-09 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:RECOVAC consortium | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Long term efficacy and safety of SARS-CoV-2 vaccination in Dutch patients with chronic kidney disease stage G4-G5, on dialysis or after kidney transplantation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: COVID-19 is associated with increased morbidity and mortality in kidney transplant recipients (KTR) and patients with chronic kidneydisease (CKD). Therefore, potential efficacious SARS-CoV-2 vaccin... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005057-31 | Sponsor Protocol Number: APO-EPO-02 | Start Date*: 2013-02-14 | |||||||||||
Sponsor Name:APOTEX Inc. | |||||||||||||
Full Title: A phase III, randomized, assessor-blinded, active-controlled, multicenter study of the efficacy and safety of APO-EPO as compared to Procrit® when given subcutaneously to patients with anemia of ch... | |||||||||||||
Medical condition: Anemia and chronic kidney disease stage 5D (patients on stable hemodialysis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) SK (Completed) BG (Completed) GR (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000765-37 | Sponsor Protocol Number: P-CKD-01 | Start Date*: 2007-05-10 | |||||||||||||||||||||
Sponsor Name:Pharmacosmos A/S | |||||||||||||||||||||||
Full Title: A non-comparative open-label study of Iron Oligosaccharide in Chronic Kidney Disease patients with a need for parenteral iron | |||||||||||||||||||||||
Medical condition: Patients with Chronic kidney disease who are in pre-dialysis or undergoing dialysis (either Peritoneal Dialysis or Haemodialysis), who may be treated with erythropoeisis stimulating agents and have... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Completed) DK (Completed) GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-006320-20 | Sponsor Protocol Number: CT.SVL.PD.10.001 | Start Date*: 2012-05-17 | |||||||||||
Sponsor Name:Synthon BV | |||||||||||||
Full Title: A multicenter, randomized, double-blind, multiple dose, crossover study to evaluate the safety and equivalence of serum phosphate control of a new sevelamer carbonate tablet formulation in compari... | |||||||||||||
Medical condition: Evaluation of the safety and equivalence of serum phosphate control of a sevelamer carbonate tablet formulation in comparison with Renvela® in chronic kidney disease patients on hemodialysis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005160-34 | Sponsor Protocol Number: MV-1-2017 | Start Date*: 2017-04-21 | |||||||||||||||||||||
Sponsor Name:Universitetsklinikken for Nyresygdomme og Blodtryksforhøjelse, Regionshospitalet Holstebro, Hospitalsenheden Vest | |||||||||||||||||||||||
Full Title: 18F-NaF PET/CT in combination with biomarkers for the classification of renal osteodystrophy in chronic kidney disease | |||||||||||||||||||||||
Medical condition: Chronic Kidney Disease - Mineral and Bone Disorder (CKD-MBD), especially renal osteodystofi. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004136-30 | Sponsor Protocol Number: 20130213 | Start Date*: 2014-03-05 | ||||||||||||||||
Sponsor Name:KAI Pharmaceuticals, Inc. (a subsidiary of Amgen, Inc.) | ||||||||||||||||||
Full Title: A Multicenter Single-arm Extension Study to Describe the Long-term Safety of AMG 416 in the Treatment of Secondary Hyperparathyroidism in Subjects With Chronic Kidney Disease on Hemodialysis | ||||||||||||||||||
Medical condition: Secondary hyperparathyroidism in subjects with chronic kidney disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) IT (Completed) BE (Completed) AT (Completed) ES (Completed) PT (Completed) LT (Completed) PL (Completed) CZ (Completed) DK (Completed) LV (Completed) DE (Completed) GR (Completed) HU (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000868-30 | Sponsor Protocol Number: NL76215.042.20 | Start Date*: 2021-02-17 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:RECOVAC consortium | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: The immune-response and safety of COVID-19 vaccination in patients with chronic kidney disease, on dialysis, or living with a kidney transplant | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: COVID-19 is associated with increased morbidity and mortality in kidney transplant recipients (KTR) and patients with chronic kidneydisease (CKD). Therefore, potential efficacious SARS-CoV-2 vaccin... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002610-13 | Sponsor Protocol Number: M11-612 | Start Date*: 2013-12-06 |
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | ||
Full Title: A Phase 3, Open-Label, Multicenter Study to Evaluate the Safety of Paricalcitol Capsules in Pediatric Subjects Ages 10 to 16 with Stage 5 Chronic Kidney Disease Receiving Peritoneal Dialysis or Hem... | ||
Medical condition: - Stage 5 chronic kidney disease - Secondary to hyperparathyroidism | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: PT (Completed) DE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005092-33 | Sponsor Protocol Number: M10-221 | Start Date*: 2008-06-10 | ||||||||||||||||
Sponsor Name:Abbott GmbH & Co. KG | ||||||||||||||||||
Full Title: The PRIMO II Study: Paricalcitol Injection benefits in Renal failure Induced cardiac Morbidity in Subjects with Chronic Kidney Disease Stage 5 | ||||||||||||||||||
Medical condition: Stage 5 Chronic Kidney Disease (CKD) in subjects receiving hemodialysis who have left ventricular hypertrophy (LVH). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) GB (Prematurely Ended) CZ (Completed) GR (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000192-33 | Sponsor Protocol Number: 20120360 | Start Date*: 2013-07-12 | ||||||||||||||||
Sponsor Name:KAI Pharmaceuticals, Inc (a subsidiary of Amgen, Inc.) | ||||||||||||||||||
Full Title: A Multicenter, Multiple-dose, Two-arm, Active-controlled, Double-blind, Double-dummy Study to Compare the Therapeutic Efficacy and Safety of Oral Doses of Cinacalcet HCl With Intravenous Doses of A... | ||||||||||||||||||
Medical condition: Chronic Kidney Disease Secondary Hyperparathyroidism (SHPT) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: PT (Completed) IT (Completed) CZ (Completed) LV (Completed) SE (Completed) AT (Completed) BE (Completed) ES (Completed) EE (Completed) DE (Completed) GR (Completed) LT (Completed) DK (Completed) HU (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-010904-27 | Sponsor Protocol Number: MK-2578-003 | Start Date*: 2009-09-07 | |||||||||||
Sponsor Name:MERCK & CO., INC. | |||||||||||||
Full Title: A Phase II Randomized, Open-Label, Multiple-Rising Dose Clinical Trial to Study the Efficacy and Safety of MK-2578 for the Maintenance of Anemia Treatment in Patients With Chronic Kidney Disease... | |||||||||||||
Medical condition: Anemia in patient with Kidney Disease (CKD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007758-70 | Sponsor Protocol Number: NH19707 | Start Date*: 2008-06-24 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: An open-label multi-center, multiple dose study to determine the optimum starting dose of intravenous MIRCERA® for maintenance treatment of anemia in pediatric patients with chronic kidney disease ... | |||||||||||||
Medical condition: Anemia associated with chronic kidney disease in pediatric patients (CKD) on hemodialysis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) FR (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002096-26 | Sponsor Protocol Number: MV-3-2017 | Start Date*: 2017-08-24 | ||||||||||||||||||||||||||
Sponsor Name:Universitetsklinik for Nyresygdomme og Blodtryksforhøjelse, Regionshospitalet Holstebro; Hospitalsenheden Vest | ||||||||||||||||||||||||||||
Full Title: Investigate the differences between treating Chronic Kidney Disease - Mineral and Bone Disorder with an iron-containing phosphate binder or a calcium-containing phosphate binder in dialysis patients. | ||||||||||||||||||||||||||||
Medical condition: Chronic Kidney Disease - Mineral and Bone Disorder (CKD-MBD), especially bone metabolism and blood vessel calcification | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002682-19 | Sponsor Protocol Number: PHI113633 | Start Date*: 2013-12-20 | |||||||||||
Sponsor Name:GlaxoSmithKline, S.A. | |||||||||||||
Full Title: A Phase 2B, randomized, blinded, dose-ranging, active-controlled, parallel-group, multi-center study to evaluate the dose response relationship of GSK1278863 over the first 4 weeks of treatment and... | |||||||||||||
Medical condition: Anemia associated with chronic kidney disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) CZ (Completed) GB (Completed) DK (Completed) HU (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001824-36 | Sponsor Protocol Number: 201201 | Start Date*: 2012-07-12 | ||||||||||||||||
Sponsor Name:Medical University of Vienna, Department of Medicine III, Division of Nephrology und Dialysis | ||||||||||||||||||
Full Title: ORAL SODIUM BICARBONATE SUPPLEMENTATION IN PATIENTS WITH CHRONIC METABOLIC ACIDOSIS AND CHRONIC KIDNEY DISEASE | ||||||||||||||||||
Medical condition: Patients classified to have chronic kidney disease of stage 3 and 4 and chronic metabolic acidosis (venous serum HCO3- of <21mml/L on 2 separate measurements at least 1 day apart) should be include... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004472-21 | Sponsor Protocol Number: PCS_03_16 | Start Date*: 2017-08-31 | |||||||||||
Sponsor Name:Pieris Pharmaceuticals GmbH | |||||||||||||
Full Title: Phase IIa study to evaluate the safety, pharmacokinetics, and pharmacodynamics of repeated administrations over 4 weeks of the hepcidin antagonist PRS-080#022-DP in anemic chronic kidney disease pa... | |||||||||||||
Medical condition: Anemia of chronic disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000541-31 | Sponsor Protocol Number: 200807 | Start Date*: 2016-12-02 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A phase 3 randomized, open-label (sponsor-blind), activecontrolled, parallel-group, multi-center, event driven study in dialysis subjects with anemia associated with chronic kidney disease to evalu... | |||||||||||||
Medical condition: Anemia associated with chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) GB (GB - no longer in EU/EEA) DK (Completed) CZ (Completed) DE (Completed) SE (Completed) PT (Completed) ES (Completed) NL (Completed) AT (Completed) GR (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002411-34 | Sponsor Protocol Number: 20140315 | Start Date*: 2019-01-28 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: Phase 3, Randomized, Open-label, Controlled, Multiple-Dose, Efficacy, Safety, Pharmacokinetic, and Pharmacodynamic Study of Etelcalcetide in Pediatric Subjects 28 days to < 18 Years of age With Sec... | |||||||||||||
Medical condition: Secondary Hyperparathyroidism (sHPT) Receiving Maintenance Haemodialysis | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
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