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Quick neck scan may predict surgery danger

NCT ID NCT07638306

What the study statuses mean

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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 Results may not be published yet.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
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Sep 11, 2026 · Updated 3 times

Summary

This study will check if a simple ultrasound of the neck vein, done before and right after anesthesia, can predict low blood pressure during surgery and kidney injury afterward. Researchers will observe 150 adults having major abdominal surgery. The goal is to see if changes in the vein's shape can warn doctors ahead of time.

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 give doctors a simple bedside test to predict and prevent dangerous low blood pressure during surgery.
What could go wrong
This is an observational study, not a treatment trial. It may not find a clear link, and results may not apply to all types of surgery or patients.

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 150 people

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

Started

Sep 2026

Expected to finish

Mar 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

Who is studied

The study population consists of adults aged 18 years and older undergoing major abdominal or visceral surgery under general anesthesia with propofol induction at the Department of Anestesiology and Intensive Care Department in the Emergency County Hospital in Târgu Mureș. Patients will be enrolled prospectively in the preoperative period if they meet eligibility criteria, have routine perioperative blood pressure monitoring, and are able to undergo internal jugular vein ultrasound before and immediately after induction. The cohort will be followed through postoperative days 1 to 3 for creatinine-based assessment of acute kidney injury.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Elective or Urgent (Non-emergent) major abdominal/ visceral surgery under general anesthesia * General anesthesia with propofol induction (TCI/ manual) * Expected surgical duration \> 60 minutes * Continous BP monitoring (Invasive arterial line or non-invasive cuff at 2 minute recording intervals) * Serum creatinine and eGFR (CKD-EPI) available within 30 days prior to surgery * Written informed consent obtained before surgery * Patient accessible by phone 30 days postoperatively Exclusion Criteria: * Emergency surgery (immediate life-saving, consent unobtainable) * End-stage renal disease (eGFR \< 15 mL/min/1.73 m²) or dialysis-dependent * Concomitant cardiac surgery or carotid endarterectomy * Liver transplantation * Known Internal Jugular Vein/ Inferior Vena Cava thrombosis or Superior Vena Cava syndrome * Any anatomical neck abnormalities precluding Internal jugular vein ultrasound * Induction with ketamine or etomidate as sole Induction agent * Neuraxial anesthesia (spinal or epidural) before propofol induction * Active decompensated heart failure (NYHA IV or acute pulmonary edema at time of Surgery) * Same-admission reoperation within 30-day study window * Withdrawal of consent at any point

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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.

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  3. A doctor treating you

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Contacts and locations

Locations

  • County Emergency Clinical Hospital of Targu Mureș

    RECRUITING

    Târgu Mureş, Mureș County, 540136, Romania

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