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NCT02114138Completed

Network Analysis of Urinary Molecular Signature Complements Clinical Data to Predict Postoperative Acute Kidney Injury

Network Analysis of Urinary Molecular Signature Complements Clinical Data to Predict Postoperative Acute Kidney Injury Subtitle: Urinary Molecular and Metabolic Signature of Postoperative Acute Kidney Injury (NavigateAKI)

Source: ClinicalTrials.gov · Last updated 7 Oct 2026

Brief summary (registry, in English)

The risk for postoperative acute kidney injury (pAKI), as for any other postoperative complications (PC), comes from a number of interactions between a patient's health before surgery, strength to tolerate surgery and influences on the operating room environment. At this time doctors do not have good tools to predict which patients may be at risk of having this complication. The purpose of this research study is to develop a urine test that can be used to predict the risk for having problems with kidney function after major surgery.

Status (registry)
Completed
Study type
Observational
Enrollment
94 (actual)
First submitted
24 Mar 2014
Start date
Jul 2015
Primary completion date
1 Dec 2025
Lead sponsor
University of Florida
NCT number
NCT02114138

What you commit to

  • Study type: Observational
  • Participants enrolled: 94
  • From Jul 2015 to the primary completion date, 1 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients not recruited 4 hours prior to undergoing surgery
  • Renal Replacement Therapy AKI/CKD Nephrectomy Organ transplant
  • Major Thoracic, abdominal, or Vascular surgery
  • Radiation Therapy
  • Chemo Therapy
  • Immunosuppressive Therapy
    • IV contrast within the past 72 hours

Other illness

  • Stroke/Transient Ischemic Attack
  • Heart Attack

Other

  • Any of the following within the last 12 months:

Who the study is looking for

  • Patients undergoing major in-hospital surgery
  • Planned hospital stay of at least 24 hours
  • Able to enroll prior to undergoing surgery
  • \> 18 years old that elect to serve as a control group

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UF Health
Coordinator of this site? Confirm its status
GainesvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.