Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Neck scan may predict dangerous drop in blood pressure during cancer surgery

NCT ID NCT07385274

Knowledge-focused Sponsor: Ankara City Hospital Bilkent Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether a simple neck ultrasound done before anesthesia can predict a dangerous drop in blood pressure after anesthesia in women having surgery for gynecologic cancer. Researchers measured blood flow in the carotid artery and checked patients' overall health and frailty. The goal was to find a non-invasive way to identify high-risk patients and improve safety during surgery.

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

91 people

The number who actually took part.

Started

Mar 2025

Finished

Sep 2025

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 adult female patients aged 18 years or older undergoing elective gynecologic oncology surgery under general anesthesia. All participants are evaluated prospectively in a single-center setting. Pre-induction carotid Doppler ultrasonography is performed as part of the perioperative assessment. Baseline comorbidity burden and frailty status are assessed using the Charlson Comorbidity Index and Clinical Frailty Scale. Patients meeting predefined inclusion and exclusion criteria are enrolled consecutively.

Ages

18 years and older

Sex

Female participants only

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: * Female patients aged 18 years or older * Scheduled for elective gynecologic oncology surgery under general anesthesia * Planned standard anesthetic induction * Ability to provide written informed consent Exclusion Criteria: * Refusal to participate in the study * Inability to obtain informed consent, including patients with dementia * Emergency surgery * American Society of Anesthesiologists (ASA) physical status IV or higher * Cardiac rhythm other than sinus rhythm * Autonomic nervous system disorders * Atrial fibrillation with rapid ventricular response * Pregnancy * Sepsis or septic shock * Significant valvular heart disease or peripheral vascular disease * Anticipated difficult ventilation and/or difficult intubation * Left ventricular ejection fraction \<40% * Severe aortic valve stenosis * Morbid obesity (body mass index \>40 kg/m²) * Presence of implanted cardiac pacemaker or implantable cardioverter-defibrillator * Chronic beta-blocker therapy * Baseline mean arterial pressure \<65 mmHg at admission * Baseline systolic arterial blood pressure \>190 mmHg or diastolic arterial blood pressure \>110 mmHg

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Gynecologic oncology patient are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

As listed by the trial registrant

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

Gynecologic oncology patient Post-induction hypotension (PIH) Ultrasonography, doppler

Contacts and locations

Locations

  • Ankara Bilkent City Hospital

    Ankara, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.