Testing of Personal Protective Equipment (PPE) for First Responders

ConditionHealthy Adult
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorMedical University of Graz

About this trial

The purpose of this pilot study is to improve protection of first responders in case of biological disasters (e.g., pandemics, biotoxin incidents). For this goal we will compare two different kinds of personal protective equipment (PPE) to be used for a variety of exercises simulating activities of first responders in the field at two different environmental temperature profiles in a randomized cross-over study design. The goal is to find the best possible compromise between protection and ergonomics as well as to determine potential factors that might limit the performance of first responders while wearing PPE. This should provide guidance for future improvement of PPE and how biosensors for monitoring heart rate and body temperature in combination with AI models may reduce risk for first responders in the field.

Eligibility criteria

Qualifiers

the KAGES hospital, Graz, Austria

the Medical University of Graz (Med Uni Graz), Austria

the University of Graz, Austria

the Red Cross

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Category III PPE suit "COMAT (Matisec, France)"
  • Category III PPE Suit "EBO-10 (EGO, Czech Republic)"

Treatment groups

12 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Medical University of Graz

Lead sponsor

European Union

Collaborator