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Simple foam dressings may shield heart surgery patients from painful bedsores

NCT ID NCT07379294

Prevention Sponsor: Shih,Wen-Chi 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether placing soft foam dressings on the skin before heart surgery can prevent pressure injuries (bedsores). About 80 adults having long heart surgeries will be enrolled. Researchers will check for new skin injuries after surgery and track how severe they are. The goal is to find a simple way to protect patients during their operation.

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

About 80 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

May 2027

An estimate. End dates often move.

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 or older * Scheduled to undergo cardiac surgery under general anesthesia * Use of cardiopulmonary bypass (CPB) during surgery * Expected surgical duration greater than 4 hours * Intact skin without pre-existing pressure injury prior to surgery Exclusion Criteria: * Surgical position other than supine * Long-term bedridden status prior to hospital admission * Altered consciousness or inability to cooperate * History of stroke with residual limb weakness

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Conditions

The condition(s) this trial relates to.

aortic aneurysm aortic disorder Aortic Dissection Aortic Valve Disease aortic valve disorder aortic valve stenosis coronary artery disorder disease heart valve disorder mitral valve disorder decubitus ulcer prevention target

As listed by the trial registrant

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

Age ≥ 18 years Aortic aneurysm Aortic diseases Aortic dissection Aortic valve diseases CABG Cad - coronary artery disease Expected surgical duration > 4 hours Intact skin preoperatively, with no existing pressure injuries Mitral disease Patients undergoing cardiac surgery under general anesthesia (E.G., avr, MVR, DVR, cabg, type A repair, bentall procedure, heart transplantation) Use of cardiopulmonary bypass (CPB) during surgery Valve disease, heart Valve heart stenosis

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  2. 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.

More trials for these conditions

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