CLINICAL TRIALS PROFILE FOR IOVERSOL
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All Clinical Trials for ioversol
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT00497328 ↗ | COmbined N-acetylcysteine and Bicarbonate in PCI To Reduce Adverse Side Effect of contrasT | Completed | National University Hospital, Singapore | Phase 2/Phase 3 | 2007-08-01 | This is a randomised controlled trial to investigate the efficacy of preventive regimen of hydration with high dose oral N-acetylcysteine and intravenous sodium bicarbonate pretreatment in patients with stable advanced renal insufficiency (CKD stage 3 and 4:GFR 15-60ml/min/1.73m2 calculated by Modification of Diet in Renal Disease Study equation (MDRD formula)) undergoing elective percutaneous coronary intervention (PCI). |
NCT00793182 ↗ | Effects of Contrast Media on Subjects With Stable Reduced Renal Function Undergoing Contrast-Enhanced Computed Tomography | Terminated | Guerbet | Phase 4 | 2009-01-01 | The purpose of this study is to evaluate the contrast-induced nephropathy (CIN) rate in subjects randomized to receive either Ioversol or Iodixanol for contrast-enhanced computed tomography. |
NCT00793182 ↗ | Effects of Contrast Media on Subjects With Stable Reduced Renal Function Undergoing Contrast-Enhanced Computed Tomography | Terminated | Mallinckrodt | Phase 4 | 2009-01-01 | The purpose of this study is to evaluate the contrast-induced nephropathy (CIN) rate in subjects randomized to receive either Ioversol or Iodixanol for contrast-enhanced computed tomography. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
Clinical Trial Conditions for ioversol
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Clinical Trial Sponsors for ioversol
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