NCT06596603Completed
Contrast-Associated Nephropathy Risk Evaluation in Acute Ischemic Stroke After Endovascular Thrombectomy
CAN-REST: Contrast-Associated Nephropathy Risk Evaluation in Acute Ischemic Stroke After Endovascular Thrombectomy
Source: ClinicalTrials.gov · Last updated 30 Jul 2025
Brief summary (registry, in English)
The CAN-REST study is a multicenter, observational, and retrospective study aimed at evaluating the incidence and risk factors of contrast-associated acute kidney injury (CA-AKI) in patients with acute ischemic stroke (AIS) who undergo endovascular thrombectomy (EVT). This study is conducted across multiple centers in Italy, Europe, the USA, and Canada, and includes data from AIS patients treated with EVT in 2023. The primary objectives are to assess the incidence of CA-AKI in this population and identify associated risk factors. Secondary objectives include evaluating the impact of CA-AKI on clinical outcomes, such as the length of hospital stay, functional recovery, and 90-day mortality, as well as developing risk stratification tools to predict CA-AKI. By analyzing a large cohort of patients, CAN-REST aims to provide critical insights into the renal complications associated with EVT and establish predictive models that can guide clinical decision-making and improve patient outcomes.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 8000 (actual)
- First submitted
- 28 Aug 2024
- Start date
- 1 Mar 2023
- Primary completion date
- 31 Dec 2024
- Lead sponsor
- Niguarda Hospital
- Diseases
- Stroke
- NCT number
- NCT06596603
What you commit to
- Study type: Observational
- Participants enrolled: 8000
- From 1 Mar 2023 to the primary completion date, 31 Dec 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- To be eligible to participate in this study, subjects must meet all of the following criteria:
- Age \>18 years at the time of AIS
- Documented serum creatinine:
- pre-EVT and
- within 48h and/or within 7 days after EVT. Patients on chronic dialysis will be collected but excluded from the analyses
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| ASST Grande Ospedale Metropolitano Niguarda Coordinator of this site? Confirm its status | Milan | Italy | Unknown status |
Related publications
This page is information, not medical advice. Discuss any trial with your doctor.