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Core Temperature in Patients With OHCA

Core Temperature in Patients With Out of Hospital Cardiac Arrest in South Tyrol - a Prospective Observational Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04976712
Acronym
CT-OCHA
Enrollment
256
Registered
2021-07-26
Start date
2021-07-01
Completion date
2027-09-30
Last updated
2026-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Accidental Hypothermia, Out-Of-Hospital Cardiac Arrest, Temperature Change, Body

Keywords

Out-Of-Hospital Cardiac Arrest, Accidental Hypothermia, Core Temperature

Brief summary

A prospective observational study aiming to monitor core temperature via an esophageal probe in out of hospital cardiac arrest during transport and until arrival in hospital. Insertion of an esophageal temperature probe will be done on scene during ongoing resuscitation manoeuvres based on European Resuscitation Council Guidelines 2015 (or newer). Environmental temperature influence and hypothermia prevention interventions will be monitored.

Detailed description

Prospective observational study to evaluate the body temperature difference in patients in out of hospital cardiac arrest on site and at arrival at the hospital. If the patient fulfills the inclusion criteria and after establishment of CPR measures according the ERC resuscitation guidelines (2015 or newer) an esophageal probe will be inserted and bodytemperature is measured; on site ambiental temperature will also be measured. Weather conditions, altitude on site, activity of the patient and hypothermia protection (eg. clothes) will bei documented. On arrival in hospital the body temperature will be measured with the esophageal probe;

Interventions

None listed

Sponsors

Azienda Sanitaria dell'Alto Adige
Lead SponsorOTHER
Institute of Mountain Emergency Medicine
CollaboratorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Out of hospital cardiac arrest * Patients transferred to hospital * \> 18 years

Exclusion criteria

* Obvious signs of death * Obvious lethal injury/injuries incompatible with life * Confirmation of death on scene * \< 18 years

Design outcomes

Primary

MeasureTime frameDescription
Core temperature at hospital arrivalthrough study completion, an average of 1 year° Celsius

Secondary

MeasureTime frameDescription
Core temperature at ROSCthrough study completion, an average of 1 year° Celsius
Environmental temperature on scenethrough study completion, an average of 1 year° Celsius
Time of resuscitation from OHCA to ROSCthrough study completion, an average of 1 yearminutes
OHCA rhythm at arrival of ALS teamthrough study completion, an average of 1 yearECG rhythm: asystolia, PEA, ventricular fibrillation, ventricular tachicardia
Use of mechanical chest compression device on prehospital interventionthrough study completion, an average of 1 year

Countries

Italy

Contacts

CONTACTRosmarie Oberhammer, MD
rosmarie.oberhammer@sabes.it00399474581660
STUDY_DIRECTORRosmarie Oberhammer, MD

Azienda Sanitaria dell'Alto Adige

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 12, 2026