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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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
ASST Grande Ospedale Metropolitano Niguarda
Coordinator of this site? Confirm its status
MilanItalyUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.