Core Temperature in Patients With OHCA

NCT ID: NCT04976712

Last Updated: 2022-12-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

256 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-07-01

Study Completion Date

2026-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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;

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

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

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Out-Of-Hospital Cardiac Arrest Accidental Hypothermia Core Temperature

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Institute of Mountain Emergency Medicine

OTHER

Sponsor Role collaborator

Azienda Sanitaria dell'Alto Adige

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Elisabeth Gruber

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Rosmarie Oberhammer, MD

Role: STUDY_DIRECTOR

Azienda Sanitaria dell'Alto Adige

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Bruneck Regional Hospital

Bruneck, , Italy

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Italy

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Rosmarie Oberhammer, MD

Role: CONTACT

Phone: 00399474581660

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Rosmarie Oberhammer, MD

Role: primary

Elisabeth Gruber, MD

Role: backup

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

BZ-107-2020

Identifier Type: -

Identifier Source: org_study_id