Can a better hazmat suit keep first responders safer and more effective?
NCT ID NCT07726537
First seen Jul 24, 2026 · Last updated Jul 24, 2026
Summary
This pilot study compares two types of Category III protective suits worn by first responders during simulated disaster-response tasks. Twelve healthy adults will perform exercises at two different temperatures while wearing each suit. Researchers will measure heart rate, body temperature, reaction time, and comfort to find the best balance between protection and performance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Category III PPE suits (COMAT and EBO-10)
- What this could lead to
- If successful, this could help design better protective gear and biosensor systems for first responders facing biological hazards.
- What could go wrong
- This is a small pilot study with only 12 participants, so results may not apply broadly. The focus is on ergonomics and monitoring, not on testing protection against actual hazards.
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
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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
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About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: The study will be open to employees or students of: * the KAGES hospital, Graz, Austria * the Medical University of Graz (Med Uni Graz), Austria * the University of Graz, Austria * the Red Cross * the Police * Fire brigade of the city of Graz Exclusion Criteria: * Pregnancy, allergy against latex or PVC, claustrophobia, acute infection, thrombophilia * Chronic illnesses (not treated) such as asthma, COPD, cardiovascular diseases, diabetes mellitus and epilepsy, * Participation in another study
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
Contacts and locations
Locations
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Medical University of Graz
RECRUITINGGraz, Styria, 8010, Austria
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