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CompletedNCT07907887TROP-AKIUpdated Oct 30, 2026

Evaluation of Postoperative Organ Injury, Risk Factors, and Short-Term Clinical Outcomes in Patients Admitted to Intensive Care After Noncardiac Surgery

An observational study in Acute Kidney Injury and Postoperative Complications, sponsored by Ankara Training and Research Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-30.

Sponsored by Ankara Training and Research Hospital · Observational

Updated Oct 30, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
224
Ages
18 Years and older
Sex
All
01

Study summary

This retrospective observational study examines whether troponin levels measured before surgery are associated with acute kidney injury during the first 48 hours after surgery in patients admitted to intensive care after noncardiac surgery. Troponin is a protein measured in blood that can indicate heart muscle injury. Acute kidney injury is a sudden decline in kidney function.

Existing medical records from 224 patients who underwent emergency or elective surgery will be reviewed. Kidney injury will be assessed using changes in blood creatinine levels and the need for dialysis or other kidney replacement therapy. The study will also examine changes in troponin levels around surgery, length of stay, and survival during hospitalization. No additional tests or treatments are performed for this study.

Read the detailed description

This single-center retrospective cohort study uses routinely collected clinical records of patients admitted to intensive care after noncardiac surgery who have available preoperative troponin measurements and postoperative kidney function data. Both emergency and elective procedures are included, and patients with chronic kidney disease are retained.

The primary objective is to evaluate the association between preoperative troponin concentration and acute kidney injury identified within 48 hours after surgery. Acute kidney injury is assessed using the serum creatinine and renal replacement therapy components of the Kidney Disease: Improving Global Outcomes criteria. Urine output criteria are not used because reliable retrospective measurements are unavailable.

Preoperative troponin is evaluated as a continuous variable and according to the laboratory upper reference limit. The main adjusted analysis accounts for age, Charlson Comorbidity Index, baseline serum creatinine, and surgical urgency. A sensitivity analysis considers chronic kidney disease status in place of baseline creatinine.

Exploratory analyses examine patterns defined by preoperative and first 24-hour postoperative troponin measurements and their association with acute kidney injury. Because troponin and creatinine measurement windows may overlap, these analyses assess associations without assuming that troponin elevation preceded kidney injury. Additional outcomes include acute kidney injury severity, renal replacement therapy, intensive care and hospital length of stay, and intensive care and hospital mortality.

The study involves no assigned intervention or additional diagnostic testing. Registration is being completed retrospectively after data collection and analysis.

02

Conditions studied

  • Acute Kidney Injury
  • Postoperative Complications

Keywords

  • Preoperative Troponin
  • Troponin T
  • Noncardiac Surgery
  • Postoperative Intensive Care
  • Retrospective Cohort Study
03

In context

Acute Kidney Injury

1,691 studies on the registry are indexed under Acute Kidney Injury; 395 are open to participants now.

This study's enrollment of 224 is above the median of 160 across 814 observational studies indexed under Acute Kidney Injury.

Browse Acute Kidney Injury studies →

Lead sponsor

Ankara Training and Research Hospital is the lead sponsor of 48 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adults aged 18 years or older who were admitted to the intensive care unit at Ankara Training and Research Hospital after emergency or elective noncardiac surgery and had preoperative troponin measurements and postoperative kidney function data available in their medical records. The retrospective cohort comprises 224 unique patients, including patients with chronic kidney disease.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18 years or older at the time of surgery.
  • Undergoing emergency or elective noncardiac surgery followed by admission to the intensive care unit.
  • Availability of a preoperative troponin measurement.
  • Availability of preoperative serum creatinine and postoperative kidney function data sufficient to assess acute kidney injury within the first 48 postoperative hours.

Exclusion criteria

Exclusion Criteria:

  • Age younger than 18 years.
  • Cardiac surgery.
  • Insufficient medical record data to assess the primary outcome.
  • Duplicate records from the same patient.
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
224 participants (actual)
Patient registry
No

Groups and cohorts

  • Noncardiac Surgery ICU Cohort

    Patients admitted to intensive care after emergency or elective noncardiac surgery who had preoperative troponin measurements and postoperative kidney function data available in their medical records. This retrospective cohort includes 224 patients. Patients with chronic kidney disease are included. No intervention was assigned as part of the study.

06

What researchers measure

Primary outcomes

  1. Acute Kidney Injury Within 48 Hours After Surgery

    Occurrence of acute kidney injury, defined by an increase in serum creatinine of at least 0.3 mg/dL within 48 hours, an increase to at least 1.5 times the preoperative baseline within the observed 48-hour period, or initiation of renal replacement therapy. Assessment uses the serum creatinine and renal replacement therapy components of KDIGO criteria. Urine output criteria are not used because reliable retrospective data are unavailable.

    Time frame: From completion of surgery through 48 hours postoperatively.

Secondary outcomes

  1. Severity of Acute Kidney Injury Within 48 Hours After Surgery

    Highest acute kidney injury stage reached within the first 48 postoperative hours, classified as KDIGO stage 1, 2, or 3 using available serum creatinine measurements and renal replacement therapy data. Initiation of renal replacement therapy is classified as stage 3. Urine output criteria are not used.

    Time frame: From completion of surgery through 48 hours postoperatively.

07

Study locations

1 site
  • Ankara Training and Research Hospital
    Ankara, Ankara 06800, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — There is currently no plan to share individual participant data.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jun 2024 to primary completion in Jun 2026, 24 months.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 26, 2026
First posted
Oct 30, 2026
StartActual
Jun 1, 2024
Primary completionActual
Jun 1, 2026
CompletionActual
Sep 30, 2026
Last update
Oct 30, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 30, 2026
Show all 1 update
  1. Oct 30, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07907887
Lead sponsor
Ankara Training and Research Hospital
Responsible party
Dilek Kuzukiran Kocatas (Principal Investigator, Ankara Training and Research Hospital) — Principal investigator
First posted
Oct 30, 2026
Start date
Jun 1, 2024
Primary completion
Jun 1, 2026
Completion
Sep 30, 2026
Last update
Oct 30, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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