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Assessing the Safety & Efficacy of RenalGuard® Therapy in the Prevention of Cardiac Surgery Associated Acute Kidney Injury (CSA-AKI) - SAFEGUARD Study
The goal of this clinical trial is to assess the effect of RenalGuard Therapy in reducing the rates of Acute Kidney Injury (AKI) within 72 hours after cardiac surgery in patients at risk of developing Cardiac Surgery Associated AKI (CSA-AKI) compared to standard-of-care (SoC). The study is planned to be conducted in 2 clinical sites in the Malaysia - Universiti Malaya Medical Centre and Institut Jantung Negara, Kuala Lumpur, Malaysia. Participants will be randomized (1:1) to one of the two study groups. The Treatment study group will be managed with the RenalGuard System. The RenalGuard treatment will start after induction of anesthesiology and will run during surgery and for 6-7 hours in the Intensive Care Unit (ICU). The treatment will aim to achieve a urine rate above a predefined urine rate threshold. Patients in the control group will be managed based on the usual clinical practice in cardiac surgery centres as detailed in the recommendations for CSA-AKI prevention by accepted clinical guidelines. For both study groups general anaesthesia, cardiopulmonary bypass (CPB) run and overall patient care will be based on SoC for cardiac surgery. Patients will be followed up for up to 7 days post surgery or until discharge, which ever comes first. Long-term follow up will be performed at 90 days post surgery.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Institut Jantung Negara
Kuala Lumpur, Malaysia
Universiti Malaya Medical Centre
Kuala Lumpur, Malaysia
Start Date
September 1, 2025
Primary Completion Date
March 31, 2027
Completion Date
June 30, 2027
Last Updated
August 14, 2025
300
ESTIMATED participants
RenalGuard® Therapy
DEVICE
Standard of Care (SOC)
OTHER
Lead Sponsor
CardioRenal Systems, Inc.
Collaborators
NCT07106151
NCT07418242
Data Source & Attribution
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