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Waking up right after heart surgery: a new anesthesia approach tested

NCT ID NCT07207421

Symptom relief Sponsor: Adiyaman University Research Hospital 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether a special 'ultra-fast-track' anesthesia method helps patients recover faster after coronary artery bypass surgery. In this approach, patients wake up and have their breathing tube removed in the operating room or within the first hour, instead of later in the ICU. The trial involved 100 adults having planned bypass surgery and measured how much heart-support medication they needed, their pain levels, and how quickly they recovered.

What this could mean

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

Active substance
Ultra-Fast-Track Anesthesia (a procedure to wake patients quickly after heart surgery)
What this could lead to
If successful, this approach could help patients recover faster after bypass surgery, with less time in the ICU and fewer heart-support drugs.
What could go wrong
This is a small, single-center study with 100 patients. Results may not apply to all heart surgery patients, and faster extubation could increase risks like breathing problems.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

100 people

The number who actually took part.

Started

Oct 2025

Finished

Dec 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.

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: * Adults aged ≥18 years undergoing elective coronary artery bypass grafting (CABG) * Patients suitable for Ultra-Fast-Track anesthesia as determined by the anesthesia team * Ability to provide written informed consent Exclusion Criteria: * Emergency CABG or combined cardiac procedures (e.g., valve surgery) * Preoperative shock or requirement for mechanical ventilation * Severe pulmonary disease (e.g., GOLD stage 3-4 COPD, home oxygen therapy) * Severe hepatic failure or end-stage renal disease requiring dialysis * Pregnancy * Inability to provide informed consent or follow-up

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Conditions

The condition(s) this trial relates to.

coronary artery disorder

As listed by the trial registrant

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

Coronary artery bypass graft (CABG) Coronary artery disease

Contacts and locations

Locations

  • Adıyaman University Training and Research Hospital

    Adıyaman, Adıyaman Province, 02200, Turkey (Türkiye)

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