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Simple blood test may flag kidney risk after bypass surgery

NCT ID NCT07445997

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study is looking at 200 people having planned heart bypass surgery to see if their blood sugar levels (HbA1c) before surgery can help predict if they will develop acute kidney injury afterward. Researchers will also use ultrasound to measure kidney blood flow. The goal is to find better ways to identify patients at risk, so doctors can take steps to protect their kidneys.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could help doctors identify patients at higher risk for kidney injury after heart bypass surgery, allowing for closer monitoring and earlier intervention.
What could go wrong
This is an observational study, not a treatment trial. It will not directly improve outcomes, and the results may not apply to all patients or surgeries.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2026

Expected to finish

Aug 2026

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

isolated coronary bypass graft surgery patients

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients undergoing isolated elective CABG surgery * Patients with available preoperative and postoperative Doppler RRI measurements * Patients with available HbA1c data Exclusion Criteria: * Patients with chronic kidney disease * Emergency surgeries * Redo/revision surgeries * Patients undergoing concomitant valve surgery * Presence of acute infection or sepsis * Advanced heart failure (EF \<30%) * Requirement for intra-aortic balloon pump, pacemaker, or mechanical circulatory support * History of nephrectomy or single kidney * Preoperative serum creatinine \>2.0 mg/dL * Pregnancy * Refusal to participate in the study

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • University of Health Sciences, Bursa Yuksek Ihtisas Training & Research Hospital

    RECRUITING

    Bursa, Turkey (Türkiye)

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