Actively Recruiting
Core Temperature in Patients With Out of Hospital Cardiac Arrest in South Tyrol - a Prospective Observational Study
Led by Azienda Sanitaria dell'Alto Adige · Updated on 2022-12-20
256
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
A
Azienda Sanitaria dell'Alto Adige
Lead Sponsor
I
Institute of Mountain Emergency Medicine
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to monitor core body temperature in patients experiencing out of hospital cardiac arrest (OHCA) during transport and upon arrival at the hospital. The study observes how environmental temperature and measures to prevent hypothermia affect these patients. It follows guidelines from the European Resuscitation Council to ensure standard resuscitation methods are applied. During the study, an esophageal temperature probe is inserted at the scene while resuscitation is ongoing to measure core temperature. Environmental factors such as weather, altitude, patient activity, and hypothermia protection like clothing are also recorded. Temperature measurements continue during transport and upon the patient's arrival at the hospital. Participants will be monitored throughout resuscitation and transport, with data collected on body temperature, environmental conditions, and resuscitation details. Researchers will track the core temperature at hospital arrival and during return of spontaneous circulation (ROSC), as well as other factors like resuscitation time and use of mechanical chest compression devices. The study collects data over about one year, focusing on temperature and resuscitation outcomes.
CONDITIONS
Brief Title
Core Temperature in Patients With OHCA
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Out of hospital cardiac arrest
- Patients transferred to hospital
- Age over 18 years
You will not qualify if you...
- Obvious signs of death
- Obvious lethal injury or injuries incompatible with life
- Confirmation of death on scene
- Age under 18 years
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit
Duration - From out of hospital cardiac arrest event until hospital arrival
Participants undergo measurement of core body temperature on site and upon hospital arrival, alongside documentation of environmental and clinical conditions during resuscitation.
1 in-person assessment on site and 1 on hospital arrival
Duration - Up to 1 year
Participants' core temperature and related clinical data are observed for up to 1 year following the cardiac arrest event.
Follow-up assessments as per routine care
Trial Site Locations
Total: 1 location
1
Bruneck Regional Hospital
Bruneck, Italy, 39031
Actively Recruiting
Research Team
R
Rosmarie Oberhammer, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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