A new care bundle aims to stop dangerous drops in body temperature after surgery

NCT ID NCT06829017

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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 Results may not be published yet.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
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Status unknown
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First seen Aug 25, 2026 · Last updated Aug 26, 2026 · Updated 1 time

Summary

This study tests a structured care bundle designed to help nurses detect, manage, and prevent postoperative hypothermia—a common complication where body temperature drops dangerously low after surgery. The bundle includes steps for diagnosing hypothermia, maintaining normal temperature, and monitoring temperature regularly. Researchers will pilot it in a cardiovascular surgery intensive care unit and measure how consistently nurses follow the bundle, aiming for at least 95% compliance.

What this could mean

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

Active substance
Postoperative Hypothermia Management Care Bundle
What this could lead to
If effective, this care bundle could become a standard approach to reduce dangerous drops in body temperature after surgery, improving patient safety and recovery.
What could go wrong
This is a small pilot study in one intensive care unit, so results may not apply broadly. Success depends on nurses consistently following the bundle, and the trial does not yet measure direct patient outcomes like complications.

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

90 people

The number who actually took part.

Started

Jan 2026

Finished

Jun 2026

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 to 85 years

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: For Nurses * Working as a nurse in Cardiovascular Surgery Intensive Care Unit for at least 6 months * Volunteering to participate in the study For patients to be cared for during the pilot implementation of the care bundle: * 18 years of age or older * Being in the first 24 hours of postoperative follow-up in the Cardiovascular Surgery Intensive Care Unit * He/she or his/her legal representative has given consent to participate in the study Exclusion Criteria: For nurses * Leaving the Cardiovascular Surgery Intensive Care Unit before the completion of the study period * Unwillingness to continue working For patients to be cared for during the piloting of the care package: \- Emergency surgical operations, patients with abnormal thermoregulation such as malignant hyperthermia and neuroleptic malignant syndrome and patients with ASA IV-V

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Hacettepe University adult hospital

    Ankara, ABD Veya Kanada'daysanız Lütfen Seçin..., 06230, Turkey (Türkiye)

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