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Study identifier: NCT07510672 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Completed

Hyperoxia vs Normoxia During Cardiopulmonary Bypass

Condition: AKI · Renal Replacement Therapy · NGAL  ·  Sponsor: University of Padova

PhaseNA
Planned participants104
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

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About this study

This single-center randomized controlled pilot trial evaluates the effects of intraoperative hyperoxia compared with normoxia during cardiopulmonary bypass (CPB) in adult patients undergoing elective cardiac surgery. The primary aim is to assess the impact on postoperative renal function. Secondary outcomes include inflammatory markers, cardiovascular and pulmonary complications, resource utilization, and short-term mortality.

This description comes directly from the study's public registry record.

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No contact information is available for this study as per the public registry record.

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Locations (1)

Padova University HospitalPadova, PD, Italy

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