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Recovery room warning signs may predict Post-Surgery dangers

NCT ID NCT06013891

Knowledge-focused Sponsor: Copenhagen University Hospital, Hvidovre 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study followed 240 high-risk surgery patients to see if problems in the recovery room (PACU) are linked to complications in the first 72 hours after leaving. Researchers tracked vital signs and medical events, and also asked nurses to assess risk. The goal is to find early warning signs that could improve patient monitoring and safety.

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 help hospitals better predict and prevent complications after surgery, improving patient safety.
What could go wrong
This is an observational study, not a treatment trial, so it won't directly change care. Results may not apply to all surgical 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

240 people

The number who actually took part.

Started

Oct 2023

Finished

Apr 2024

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

We will include approximately 250 adults undergoing surgery for hip fracture, lower limb amputation, open liver resection, open pancreatic and esophageal/gastric surgery, and open or laparoscopic major abdominal surgery. The surgical patient categories are selected based on types of surgery performed at the research sites, clinical experience, and well-known high risks of postoperative morbidity and mortality.

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.

Patients who wish to participate will sign a consent form. Baseline data will be obtained on all eligible participants; however, the full registry will only be obtained for those who permit us. To recruit participants, the surgical schedules will be screened on a daily basis by the principal investigator and/or a member of the research team (VB). Data entry has been prepared in RedCap, a secure method of robust data collection. All data entry will be reviewed and validated by LBH and VB. In case of discrepancies or inconsistencies, senior members of the research team NBF or EKA will review data for clarity and validation. Inclusion Criteria: -Adult patients undergoing surgery for a hip fracture, lower limb amputation, open liver resection, open pancreatic, and esophageal/gastric surgery And * Adult patients undergoing open or laparoscopic major abdominal surgery and orthopedic surgery * Surgery time over 2 hours * American Society of Anesthesiologists (ASA) physical status classification system 3 - 4 Exclusion Criteria: * Pre-planned fixed minimum PACU stay * Planned intensive care unit (ICU) stay * Terminally ill * Incapable of giving informed consent

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Conditions

The condition(s) this trial relates to.

Clinical Deterioration Postoperative Complications

As listed by the trial registrant

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

Anesthesiology Deterioration, clinical Postoperative care Postoperative complications

Contacts and locations

Locations

  • Amager and Hviovre Universitu Hospital

    Hvidovre, 2650, Denmark

More trials for these conditions

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