A Study to Explore the Renal Safety of Visipaque Injection 320 mgI/mL in Patients With Chronic Kidney Disease
Parallel-Group, Placebo-Controlled Randomized Study Investigating the Effect of Intravenous Iso-osmolar Iodinated Contrast Material Iodixanol (Visipaque™ Injection 320 mgI/mL) on Renal Function in Adults With Chronic Kidney Disease (CKD) Stage III or Stage IV Who Have Undergone Endovascular Aneurysm Repair (EVAR)
Sponsor: GE Healthcare
Terminated
The trial was discontinued due to a lower than anticipated recruitment rate. The decision has not been made due to any safety reasons.
A PHASE4 clinical study on Chronic Kidney Diseases, this trial is terminated or withdrawn. The trial is conducted by GE Healthcare and has accumulated 18 data snapshots since 2018. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
18 versions recorded-
Sep 2025 — Present [monthly]
Terminated PHASE4
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Sep 2024 — Sep 2025 [monthly]
Terminated PHASE4
-
Jul 2024 — Sep 2024 [monthly]
Terminated PHASE4
-
Dec 2021 — Jul 2024 [monthly]
Terminated PHASE4
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Jan 2021 — Dec 2021 [monthly]
Terminated PHASE4
▶ Show 13 earlier versions
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Nov 2020 — Jan 2021 [monthly]
Terminated PHASE4
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Jan 2020 — Nov 2020 [monthly]
Terminated PHASE4
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Nov 2018 — Jan 2020 [monthly]
Terminated PHASE4
Status: Recruiting → Terminated
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Oct 2018 — Nov 2018 [monthly]
Recruiting PHASE4
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Sep 2018 — Oct 2018 [monthly]
Recruiting PHASE4
-
Aug 2018 — Sep 2018 [monthly]
Recruiting PHASE4
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Jul 2018 — Aug 2018 [monthly]
Recruiting PHASE4
-
Jun 2018 — Jul 2018 [monthly]
Recruiting PHASE4
-
May 2018 — Jun 2018 [monthly]
Recruiting PHASE4
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Mar 2018 — May 2018 [monthly]
Recruiting PHASE4
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Feb 2018 — Mar 2018 [monthly]
Recruiting PHASE4
-
Dec 2017 — Feb 2018 [monthly]
Recruiting PHASE4
Status: Not Yet Recruiting → Recruiting
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May 2017 — Dec 2017 [monthly]
Not Yet Recruiting PHASE4
First recorded
Eligibility Summary
No eligibility information available.
Contact Information
- GE Healthcare
- Syneos Health
For direct contact, visit the study record on ClinicalTrials.gov .