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Plastic dome over Patients' heads tested as airborne germ barrier

NCT ID NCT06968377

Prevention Sponsor: IWK Health Centre 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 16, 2026 · Last updated Sep 17, 2026 · Updated 1 time

Summary

Researchers are testing a clear plastic dome placed over a patient's head during surgery to see if it can stop the spread of airborne germs in hospitals. The trial enrolls 80 adults having elective surgery that requires a breathing tube. Participants are randomly assigned to have the dome or not, and researchers compare how long it takes to place the breathing tube, patients' oxygen levels and heart rate, and how patients feel about the device.

What this could mean

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

Active substance
a clear plastic dome placed over the patient's head during surgery
What this could lead to
If the dome works, hospitals could have a simple barrier that reduces airborne infection spread during surgery. It might also protect health care workers from aerosols released during breathing tube placement.
What could go wrong
The dome could make breathing tube placement slower or harder, or cause discomfort. This is an early study with 80 patients, so it cannot show whether the device actually prevents infections.

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.

Started

Jan 2026

Expected to finish

Apr 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

Accepted

You do not need to have the condition being studied to take part.

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: * ASA class 1 and 2 * Elective surgery * Adults \>18 years of age * Ability to give informed consent * Surgery in supine or lithotomy position * Surgical site: abdominal, pelvic, lower limb or distal upper limb * Endotracheal intubation is indicated as per attending anesthesiologist Exclusion Criteria: * BMI \>40 * pregnancy * "full stomach" or increased intraabdominal pressure (as per attending anesthesiologist) * predictors of difficult airway management as per attending anesthesiologist * airway management plan (as per attending anesthesiologist) that is incompatible with study protocol * initial ventilatory settings that are incompatible with planned care as per study protocol * Claustrophobia * significant cardiovascular or respiratory disease (including pleural effusion, pulmonary edema, etc.) * anticipated significant level of post-operative sedation preventing survey participation

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Conditions

The condition(s) this trial relates to.

COVID-19 prevention target

As listed by the trial registrant

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

Aerosol generating procedure Medical device Medical device performance

How to take part

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  1. The study's own enquiry address

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  2. The places running it

    1 site. The list below names each one and where it is.

  3. 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 ↗

  4. A doctor treating you

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Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

Locations

  • IWK Health Centre

    RECRUITING

    Halifax, Nova Scotia, B3K 6R8, Canada

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