- Trials with a EudraCT protocol (125)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
125 result(s) found for: Clinical epidemiology.
Displaying page 1 of 7.
EudraCT Number: 2014-003818-92 | Sponsor Protocol Number: CURITIBA_TRIAL | Start Date*: 2014-12-22 | |||||||||||
Sponsor Name:Ospedale San Raffaele, UO Chirurgia Vascolare | |||||||||||||
Full Title: CUstodiol vs RInger: whaT Is the Best Agent? | |||||||||||||
Medical condition: Thoracoabdominal aortic aneurysm | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005342-63 | Sponsor Protocol Number: UoL001206 | Start Date*: 2016-06-23 |
Sponsor Name:University of Liverpool | ||
Full Title: Mindex: The efficacy and safety of very low dose dexamethasone used to facilitate the extubation of ventilator dependent preterm babies who are at high risk of bronchopulmonary dysplasia | ||
Medical condition: Bronchopulmonary dysplasia | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004084-12 | Sponsor Protocol Number: EFC15392 | Start Date*: 2018-07-10 | |||||||||||
Sponsor Name:Genzyme Corporation | |||||||||||||
Full Title: Multicenter, Randomized, Double-blind, Placebo-controlled Two Stage Study to Characterize the Efficacy, Safety, Tolerability and Pharmacokinetics of GZ/SAR402671 in Patients at risk of Rapidly Prog... | |||||||||||||
Medical condition: Congenital, hereditary and neonatal diseases | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) DK (Completed) GB (GB - no longer in EU/EEA) BE (Prematurely Ended) ES (Prematurely Ended) NL (Completed) PT (Prematurely Ended) CZ (Prematurely Ended) AT (Prematurely Ended) IT (Prematurely Ended) RO (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000656-26 | Sponsor Protocol Number: BAY1142524/18933 | Start Date*: 2017-11-29 |
Sponsor Name:Bayer AG | ||
Full Title: A randomized, double-blind, multicenter study to assess the efficacy and safety of a 6 month oral treatment with the chymase inhibitor BAY 1142524 at a dose of 25 mg BID in comparison to placebo ... | ||
Medical condition: type II diabetic mellitus (T2DM) patients with a clinical diagnosis of diabetic kidney disease (CKD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) FI (Completed) DK (Completed) ES (Completed) BG (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-005583-25 | Sponsor Protocol Number: COLIMERO | Start Date*: 2014-07-16 |
Sponsor Name:Consorci Parc de Salut Mar de Barcelona | ||
Full Title: Multicenter, randomized, open label, controlled clinical trial that compares the efficacy of the combination of colistin and meropenem versus monotherapy for the treatment of bacteremia and pneumon... | ||
Medical condition: Bacteriemia and Pneumonia due to Pseudomonas aeruginosa | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-016566-82 | Sponsor Protocol Number: 05/SP/120 | Start Date*: 2009-12-29 |
Sponsor Name:Belfast Health and Social Care Trust [...] | ||
Full Title: Skin bacteria as a source of surgical infections: molecular epidemiology and prevention of wound contaimination | ||
Medical condition: No medical condition under investigation, investigation of surgical wound contamination in spinal patients. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000315-24 | Sponsor Protocol Number: 1208182 | Start Date*: 2013-06-18 | ||||||||||||||||
Sponsor Name:CHU SAINT-ETIENNE | ||||||||||||||||||
Full Title: Pharmaco-epidemiology of the treatment of the symptomatic pulmonary embolism among in-patients and 75 years old or more: prospective, multicentric "PEAGE" cohort | ||||||||||||||||||
Medical condition: Symptomatic pulmunory embolism on patients over 75 years | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004511-31 | Sponsor Protocol Number: cASPerCF_2007_OPBG_2019 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Bambino Gesù Children's Hospital | |||||||||||||
Full Title: Prospective validation and clinical evaluation of a new posaconazole dosing regimen for children and adolescents with cystic fibrosis and Aspergillus infection. | |||||||||||||
Medical condition: Cystic Fibrosis and Aspergillus Infection | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IT (Prematurely Ended) PT (Prematurely Ended) GR (Prematurely Ended) FR (Prematurely Ended) NL (Prematurely Ended) IE (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002319-43 | Sponsor Protocol Number: APHP200020 | Start Date*: 2022-11-17 |
Sponsor Name:Assistance Publique - Hôpitaux de Paris | ||
Full Title: Efficacy of 7 days versus 14 days of antibiotic therapy for acute pyelonephritis in kidney transplant recipients, a multicentre randomized non-inferiority trial. | ||
Medical condition: Kidney Transplant recipient with acute pyelonephritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003084-26 | Sponsor Protocol Number: CHK0101 | Start Date*: 2021-04-08 |
Sponsor Name:Chinook Therapeutics U.S., Inc. | ||
Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study of Atrasentan in Patients with IgA Nephropathy at Risk of Progressive Loss of Renal Function (The ALIGN Study) | ||
Medical condition: Immunoglobulin A Nephropathy (IgAN) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) PL (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) CZ (Completed) IE (Completed) PT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000619-42 | Sponsor Protocol Number: PI14/00638 | Start Date*: 2015-05-05 |
Sponsor Name:FIBICO | ||
Full Title: An open, Phase II, clinical trial to evaluate the effectiveness of decreased intestinal absorption of phosphorus in the progression of renal disease in patients with metabolic syndrome | ||
Medical condition: Chronic kidney disease and metabolic syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012283-14 | Sponsor Protocol Number: SECOND-LINE | Start Date*: 2010-08-16 | |||||||||||
Sponsor Name:National Centre in HIV Epidemiology and Clinical Research | |||||||||||||
Full Title: A randomised open‐label study comparing the safety and efficacy of ritonavir boosted lopinavir and 2‐3N(t)RTI backbone versus ritonavir boosted lopinavir and raltegravir in participants virological... | |||||||||||||
Medical condition: Chronic HIV infection | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) FR (Ongoing) GB (Completed) DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004260-22 | Sponsor Protocol Number: ELFIN01 | Start Date*: 2013-08-28 |
Sponsor Name:University of Oxford | ||
Full Title: A multi-centre randomised placebo-controlled trial of prophylactic enteral lactoferrin supplementation to prevent late-onset invasive infection in very preterm infants. | ||
Medical condition: Late onset invasive infection in very preterm infants | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-002140-51 | Sponsor Protocol Number: INV-CL-106 | Start Date*: 2022-12-21 | |||||||||||
Sponsor Name:Inversago Pharma Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study of the Efficacy, Safety, and Pharmacokinetics of Two Doses of INV-202 in Patients with Diabetic Kidney Disease | |||||||||||||
Medical condition: Diabetic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003819-22 | Sponsor Protocol Number: ID-080A305 | Start Date*: 2019-11-07 |
Sponsor Name:Idorsia Pharmaceuticals Ltd | ||
Full Title: Multi-center, blinded, randomized study with aprocitentan in subjects with uncontrolled blood pressure and chronic kidney disease stage 3 or 4. | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) LV (Prematurely Ended) ES (Prematurely Ended) CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-004400-34 | Sponsor Protocol Number: LTS15823 | Start Date*: 2021-03-23 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
Full Title: Multicenter, open-label, extension study to characterize the long-term efficacy and safety of early versus delayed treatment with venglustat (GZ/SAR402671) in patients at risk of rapidly progressiv... | |||||||||||||
Medical condition: Congenital cystic kidney disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) NL (Completed) BE (Prematurely Ended) DE (Completed) PT (Prematurely Ended) IT (Prematurely Ended) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002637-15 | Sponsor Protocol Number: APL2-C3G-204 | Start Date*: 2020-12-22 |
Sponsor Name:Apellis Pharmaceuticals, Inc. | ||
Full Title: AN OPEN-LABEL, RANDOMIZED, CONTROLLED, PHASE 2 STUDY TO EVALUATE THE SAFETY AND EFFICACY OF PEGCETACOPLAN IN THE TREATMENT OF POST-TRANSPLANT RECURRENCE OF C3G OR IC‑MPGN | ||
Medical condition: complement 3 glomerulopathy (C3G)/immune complex membranoproliferative glomerulonephritis (IC-MPGN) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) AT (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) FR (Completed) IT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003527-14 | Sponsor Protocol Number: D9480C00023 | Start Date*: 2021-12-17 | |||||||||||
Sponsor Name:ASTRAZENECA AB | |||||||||||||
Full Title: An Open-Label, Randomised, Phase 4 Study of Continuing Sodium Zirconium Cyclosilicate (SZC) after Discharge in Participants with Chronic Kidney Disease treated for Hyperkalaemia | |||||||||||||
Medical condition: Patients with Chronic Kidney Disease treated for Hyperkalaemia whilst in hospital, who are normokalemic and established on maintenance dose of SZC at discharge. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Ongoing) FR (Completed) NL (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006579-41 | Sponsor Protocol Number: ANG3070-CKD-201 | Start Date*: 2022-03-07 | |||||||||||
Sponsor Name:Angion Biomedica Corp. | |||||||||||||
Full Title: A Phase 2, Multicenter, Double-Blind, Randomized, Placebo-controlled Study of Safety and Efficacy Of ANG-3070 in Patients with Primary Glomerular Disease and Persistent Proteinuria | |||||||||||||
Medical condition: Primary glomerular disease and persistent proteinuria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) ES (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000185-42 | Sponsor Protocol Number: VX19-147-101 | Start Date*: 2020-06-01 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 2a, Open-label, Single-arm, 2-Part Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of VX-147 in Adults With APOL1-mediated Focal Segmental Glomerulosclerosis. | |||||||||||||
Medical condition: APOL1-mediated Focal segmental glomerulosclerosis (FSGS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) | |||||||||||||
Trial results: View results |
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