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Cystatin and Early AKI Detection Contrast Induced Acute Kidney Injury

B

BayCare Health System

Status

Enrolling

Conditions

Acute Kidney Injury

Study type

Observational

Funder types

Other

Identifiers

NCT07197957
Cystatin & Early AKI Detection

Details and patient eligibility

About

To determine the clinical utility of serum cystatin C in early detection of acute kidney injury (AKI).

Full description

The primary objective of this study is to evaluate the clinical utility of Cystatin C in early detection of contrast-induced AKI.

To evaluate the effect of patient characteristics in the Cystatin C based GFR estimation in comparison to Cr based estimation.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects ages 18 years and above
  • Inpatients with CKD (Figure 1)
  • Order for CT imaging study or coronary angiography with isohexol Omnipaque) contrast media.
  • Pre and post contrast available
  • All races and ethnicity of patients are eligible. We expect to analyze approximately equal number of men and women in this study.

Exclusion criteria

  • Preexisting dialysis
  • Patients under the age of 18 years
  • Pregnancy
  • Incarcerated individuals
  • Patients with impaired cognition and unable to follow consent procedures
  • Recent exposure to CM (within 2 days before/after procedure)
  • Cardiac shock
  • Medications that affect biomarkers, including corticosteroids, lfamethoxazoletrimethoprim

Trial contacts and locations

4

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Central trial contact

Tracy Johns, PharmD

Data sourced from clinicaltrials.gov

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