Skip to content
Study details
Enrolling now

Comparison of Early Proton Pump Inhibitor Initiation Versus Usual Care on Acute Kidney Injury in Hemorrhagic Shock Patients

The University of Texas Health Science Center, Houston
NCT IDNCT06531642ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2/3

Target enrollment

100

Study length

about 11 months

Ages

18+

Locations

1 site in TX

What this study is about

Researchers are testing whether starting a proton pump inhibitor (PPI) medication early after an injury can help prevent acute kidney injury (AKI) in people who have experienced hemorrhagic shock. The trial will compare this approach to the usual way of starting PPIs, which is later on. Kidney injury will be assessed by measuring specific biomarkers in urine and tracking the incidence, severity, and AKI-free days within the first week, as well as major adverse kidney events (MAKE) at day 30.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Protonix (Pantoprazole) 40 mg q 12 hrs for 2 days
  • 2.Take Protonix (pantoprazole) 40 mg q 24 hrs for 2 days

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

pantoprazole

Drug routes

oral (Delayed Release Oral Tablet)

Endpoints

Primary: Urinary Kidney Biomarker Levels

Body systems

Renal