Cure My Disease

Don't miss your cure!

 Log in / Sign up

Can doctors foresee which patients need intensive care?

NCT ID NCT07780526

Knowledge-focused Sponsor: Van Training and Research Hospital Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 21, 2026 · Last updated Sep 01, 2026 · Updated 2 times

Summary

This study asks whether anesthesiologists can accurately predict, before a procedure, if an adult patient will need intensive care afterward. Researchers will compare the doctors' predictions with actual ICU admissions within 24 hours after surgery or endoscopy. The study is observational, meaning it does not change patient care, and also checks if the data collection process is practical for a larger future study.

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 accurate, this could improve how doctors plan postoperative care, potentially reducing unplanned ICU admissions and better allocating resources.
What could go wrong
This is a small pilot study, so results may not be conclusive. Prediction accuracy could vary widely among anesthesiologists, and the findings may not apply to all hospitals or patient groups.

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 100 people

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

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Sep 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

The study population will consist of adult patients undergoing eligible surgical or endoscopic procedures in the participating operating rooms and endoscopy units on the predefined study days. Patients with The american society of anesthesiologists (ASA) Physical Status of I-II will be included if they undergo a major procedure, while patients with ASA Physical Status of III-V will be considered for inclusion regardless of procedural magnitude, provided that all other eligibility criteria are met. Preoperative clinical assessment will be completed before the procedure, and postoperative outcomes will be recorded prospectively.

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.

İnclusion Criteria: * Age 18 years or older. * Undergoing an eligible surgical or endoscopic procedure on a predefined study day. * The american society of anesthesiologists (ASA) Physical Status of I-II and undergoing a major surgical or endoscopic procedure, or ASA Physical Status of III-V and undergoing an eligible surgical or endoscopic procedure. * Preoperative anesthesiology assessment completed before the procedure. Exclusion Criteria: * Age younger than 18 years. * ASA Physical Status of I-II and undergoing a minor or non-major procedure. * Undergoing cardiac surgery. * Already admitted to an intensive care unit before the index procedure. * The planned surgical or endoscopic procedure is not ultimately performed. * The required preoperative assessment cannot be completed before the procedure.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Perioperative risk assessment are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

As listed by the trial registrant

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

Perioperative risk assessment Postoperative intensive care unit admission

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

  • Van Education and Research Hospital

    RECRUITING

    Van, Turkey (Türkiye)

More trials for these conditions

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