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Study identifier: NCT05805709 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Patient-centered Trial of a Process-of-care Intervention in Hospitalized AKI Patients: the COPE-AKI Trial

Condition: Acute Kidney Injury  ·  Sponsor: University of Pittsburgh

PhaseNA
Planned participants2145
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The COPE-AKI study is a randomized, pragmatic, parallel-arm trial comparing a multimodal intervention to usual care on hospital-free days through 90 days of study follow up. The primary study hypothesis is that patients randomized to the intervention will have increased odds of more hospital-free days through 90 days (primary clinical) compared to those randomized to usual care. Key secondary hypotheses will investigate the impact of the intervention on rates of major adverse kidney events, rates of recurrent AKI, and changes in patient-reported outcomes. Participants (N=2145) will be allocated 1:1 to the intervention or usual care using a web-based system to maintain allocation concealment using stratified randomization with randomly permuted blocks. Randomization will be stratified by clinical site.

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

Talk to the study team

Susan J Copelli, MSHI  ·  412-245-0803  ·  sju1@pitt.edu

Kaleab Abebe, PhD  ·  kza3@pitt.edu

Always discuss trial participation with your own doctor first.

Locations (9)

University of Alabama at BirminghamBirmingham, Alabama, United StatesRecruiting
Yale UniversityNew Haven, Connecticut, United StatesRecruiting
Cleveland Clinic Weston HospitalWeston, Florida, United StatesRecruiting
University of MarylandBaltimore, Maryland, United StatesRecruiting
Johns Hopkins UniversityBaltimore, Maryland, United StatesRecruiting
MetroHealthCleveland, Ohio, United StatesRecruiting
Cleveland Clinic FoundationCleveland, Ohio, United StatesRecruiting
Nashville VA Medical CenterNashville, Tennessee, United StatesRecruiting
Vanderbilt UniversityNashville, Tennessee, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05805709