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Study identifier: NCT06706258 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Post-Cardiac Surgery Acute Kidney Injury Prevention by Administration of Proton Pump Inhibitor (P2 Trial)

Condition: Acute Kidney Injury  ·  Sponsor: The University of Texas Health Science Center, Houston

PhasePhase 2
Planned participants400
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

The central hypothesis of this research study is that perioperative administration of the proton pump inhibitor (PPI) pantoprazole could reduce the development of acute kidney injury (AKI) following cardiac surgery by activation molecular pathways for kidney protection. The investigators propose a single-center, randomized, controlled, single-blinded trial to determine whether perioperative intravenous administration of pantoprazole will reduce the incidence of AKI, some molecules that can be detected the urine, and major adverse kidney events (MAKE) at day 30 postoperatively, compared to famotidine after cardiac surgery. The specific aims of the study will be achieved by randomizing a group of 400 patients to receive pantoprazole (study) or famotidine (control) for 3 days perioperatively. Our study population will include any adult patients (aged over 18 years) scheduled for cardiac surgery requiring a cardiopulmonary bypass machine.

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

Talk to the study team

Yafen Liang, MD  ·  713-500-6226  ·  yafen.liang@uth.tmc.edu

Simon Betancourt Escobar, MD  ·  713-500-5739  ·  simon.betancourtescobar.1@uth.tmc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Memorial Hermann Texas Medical CenterHouston, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06706258