- Trials with a EudraCT protocol (73)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
73 result(s) found for: Renal threshold.
Displaying page 1 of 4.
EudraCT Number: 2017-002443-15 | Sponsor Protocol Number: ICAF-BETA | Start Date*: 2017-09-20 | |||||||||||
Sponsor Name:York Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Improving cardiac function in high-risk surgical patients: exercise testing, biomarkers and beta-blockade | |||||||||||||
Medical condition: Impaired VE/CO2 on cardio pulmonary exercise testing | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010190-20 | Sponsor Protocol Number: 0908010 | Start Date*: 2009-04-22 | |||||||||||
Sponsor Name:CHU Saint-Etienne | |||||||||||||
Full Title: DETECTION OF ACUTE RENAL FAILURE IN CRITICALLY ILL PATIENTS: A prospective evaluation of cystatin C diagnostic performance | |||||||||||||
Medical condition: critically ill patients hospitalised in inetnsive care unit | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006948-65 | Sponsor Protocol Number: Version 4 | Start Date*: 2007-11-29 |
Sponsor Name:University Hospitals of Leicester NHS Trust | ||
Full Title: The effect of acidosis correction and exercise on tissue wasting and immune function in renal patients | ||
Medical condition: Chronic kidney disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001510-42 | Sponsor Protocol Number: RC19_0133 | Start Date*: 2019-11-25 | |||||||||||
Sponsor Name:CHU de Nantes | |||||||||||||
Full Title: Interest of belatacept as a non-nephrotoxic immunosuppressive treatment in cardiac transplant patients at risk of chronic renal failure. | |||||||||||||
Medical condition: Early graft dysfunction after heart transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004272-11 | Sponsor Protocol Number: 2B | Start Date*: 2011-11-30 |
Sponsor Name:Erasmus MC | ||
Full Title: The BOKITO-2B Study: Tenofovir DF Bone and Kidney Toxicity. Incidence and reversibility in HBV-monoinfected patients. | ||
Medical condition: Chronic hepatitis B | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016653-17 | Sponsor Protocol Number: FARM73452X | Start Date*: 2010-04-13 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA UNITA` SANITARIA LOCALE N 12 DI VIAREGGIO | ||||||||||||||||||||||||||||
Full Title: TREATMENT OF HYPOTENSION IN EXTREMELY PRETERM INFANTS: A MULTICENTER RANDOMIZED CONTROLLED TRIAL | ||||||||||||||||||||||||||||
Medical condition: HYPOTENSION IN EXTREMELY PRETERM INFANTS | ||||||||||||||||||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005468-10 | Sponsor Protocol Number: C16011 | Start Date*: 2012-11-28 |
Sponsor Name:Millennium Pharmaceuticals, Inc. | ||
Full Title: A Phase 3 Randomized, Controlled, Open-label, Multicenter, Safety and Efficacy Study of Dexamethasone Plus MLN9708 or Physician's Choice of Treatment Administered to Patients With Relapsed or Refra... | ||
Medical condition: Relapsed or Refractory Systemic Light Chain (AL) Amyloidosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) NL (Completed) GB (Prematurely Ended) IT (Completed) GR (Completed) ES (Prematurely Ended) DK (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003472-19 | Sponsor Protocol Number: version 4.0, 31 May 2007 | Start Date*: 2007-09-13 |
Sponsor Name:Royal Free Hampstead NHS Trust | ||
Full Title: Determining a viral load threshold for pre-emptive therapy for cytomegalovirus infection in transplant patients using real time PCR monitoring. | ||
Medical condition: Transplant recipients with CMV infection. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000201-23 | Sponsor Protocol Number: reflect01 | Start Date*: 2013-08-30 |
Sponsor Name:St. Antonius Ziekenhuis | ||
Full Title: A randomised clinical trial evaluating the effect of remifentanil vs fentanyl during cardiac surgery on the incidence of chronic thoracic pain. | ||
Medical condition: chronic thoracic pain after cardiac surgery via sternotomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005793-63 | Sponsor Protocol Number: CLIK066A2202 | Start Date*: 2013-10-30 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A multi-center, randomized, double-blind, double-dummy, parallel-group dose-finding study to evaluate the change in HbA1c after 12 weeks monotherapy with seven doses of LIK066 compared with placebo... | ||
Medical condition: Type II Diabetes mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) SK (Prematurely Ended) IT (Prematurely Ended) PL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-005830-14 | Sponsor Protocol Number: CVAY736K12301 | Start Date*: 2022-07-04 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, double-blind, parallel group, placebo-controlled, multicenter Phase 3 trial to evaluate the efficacy, safety and tolerability of ianalumab on top of standard-of-care therapy in patien... | |||||||||||||
Medical condition: Lupus nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) HU (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) CZ (Trial now transitioned) EE (Trial now transitioned) LT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004201-25 | Sponsor Protocol Number: 1B | Start Date*: 2011-11-30 |
Sponsor Name:Erasmus MC | ||
Full Title: The BOKITO-1B Study: Tenofovir DF Bone and Kidney Toxicity. Pharmacology in HBV monoinfected patients. | ||
Medical condition: Chronic hepatitis B | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001377-31 | Sponsor Protocol Number: HZNP-DAX-203 | Start Date*: 2022-12-09 | |||||||||||
Sponsor Name:Horizon Therapeutics Ireland DAC | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PHASE 2 STUDY EVALUATING THE EFFICACY AND SAFETY OF DAXDILIMAB IN ADULT PARTICIPANTS WITH ACTIVE PROLIFERATIVE LUPUS NEPHRITIS | |||||||||||||
Medical condition: ACTIVE PROLIFERATIVE LUPUS NEPHRITIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002556-39 | Sponsor Protocol Number: 2020/0422/HP | Start Date*: 2022-11-28 |
Sponsor Name:DRCI - CHU de Rouen | ||
Full Title: Efficacy of a preventive strategy for immuno-guided cytomegalovirus infection compared to a universal prophylactic strategy in renal transplant recipients | ||
Medical condition: Patients receiving a kidney transplant (1 to 12 days post-transplant) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003867-79 | Sponsor Protocol Number: IDTX-MA-3004 | Start Date*: 2018-11-07 | |||||||||||
Sponsor Name:Astellas Pharma Global Development, Inc. | |||||||||||||
Full Title: Astagraf XL® to Understand the Impact of Immunosuppression on De Novo DSA Development and Chronic Immune Activation in Kidney Transplantation | |||||||||||||
Medical condition: Understand the Impact of Immunosuppression on De Novo DSA Development and Chronic Immune Activation in Kidney Transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002957-42 | Sponsor Protocol Number: EMR200592-001 | Start Date*: 2013-08-06 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: A Randomized, Double-Blind, Phase III Study of the Efficacy and Safety of Gemcitabine in Combination With TH-302 Compared With Gemcitabine in Combination With Placebo in Previously Untreated Subjec... | |||||||||||||
Medical condition: Locally advanced unresectable pancreatic adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) CZ (Prematurely Ended) DE (Completed) HU (Completed) ES (Completed) SK (Completed) IT (Completed) PL (Completed) FI (Completed) NL (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002843-81 | Sponsor Protocol Number: 057 | Start Date*: 2020-01-07 |
Sponsor Name:IMEA | ||
Full Title: Switch to Tenofovir Alafenamide (TAF), Emtricitabine (FTC), Bictegravir (BIC)(Biktarvy®) in HIV-1-infected patients over 65 years old at risk of polymedication | ||
Medical condition: HIV-1-infected patient Age > 65 years old Plasma HIV RNA ≤ 50 copies/mL for ≥ 6 months: one blip between 50 et 200 cp/ml is allowed in the last 6 months before screening. Currently receiving an ant... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002151-10 | Sponsor Protocol Number: NEUROPROTECTpost-CA | Start Date*: 2015-08-07 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: Neuroprotective goal directed hemodynamic optimization in post-cardiac arrest patients: a randomized controlled trial (the NEUROPROTECT post-CA trial) | |||||||||||||
Medical condition: post-cardiac arrest patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001457-43 | Sponsor Protocol Number: APHP200388 | Start Date*: 2020-04-10 |
Sponsor Name:APHP | ||
Full Title: Dexamethasone and oxygen support strategies in ICU patients with Covid-19 pneumonia | ||
Medical condition: acute hypoxemic respiratory failure (AHRF) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002927-40 | Sponsor Protocol Number: ANAM-17-21 | Start Date*: 2019-06-19 |
Sponsor Name:Helsinn Healthcare SA | ||
Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Anamorelin HCl for the Treatment of Malignancy Associated Weight Loss and Anorexia i... | ||
Medical condition: Treatment of malignancy associated weight loss or anorexia in patients with NSCLC | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) BE (Completed) PL (Completed) HR (Completed) RO (Ongoing) | ||
Trial results: View results |
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