Quick neck scan may predict surgery danger
NCT ID NCT07638306
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
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2026
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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.
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The places running it
1 site. The list below names each one and where it is.
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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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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
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County Emergency Clinical Hospital of Targu Mureș
RECRUITINGTârgu Mureş, Mureș County, 540136, Romania
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