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Feedback Intervention and Treatment Trial in Patients With Out-of-Hospital Cardiac Arrest

Feedback Intervention and Treatment Trial in Patients With Out-of-Hospital Cardiac Arrest (FITT-OHCA)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06299969
Acronym
FITT-OHCA
Enrollment
3000
Registered
2024-03-08
Start date
2023-01-01
Completion date
2025-12-31
Last updated
2024-03-08

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

Conditions

Out-Of-Hospital Cardiac Arrest

Keywords

OHCA, Out-of-hospital cardiac arrest, In-hospital cardiac arrest, Resuscitation, Cardiac arrest center, Feedback intervention, Acute care medicine

Brief summary

The trial collects and analyzes data from Cardiac Arrest Centres in patients with out-of-hospital cardiac arrest (OHCA).

Detailed description

With around 70,000 cases per year, out-of-hospital cardiac arrest (OHCA) is one of the most common causes of death in Germany. Only less than 10% of patients with an OHCA can currently be discharged with a satisfactory neurological outcome. The FITT-OHCA trial is a quality management project and collects data from Cardiac Arrest Centres on pre-hospital care and early post-resuscitation treatment in a standardized manner. The aim is to optimize the treatment process in patients following successful prehospital resuscitation through systematic data collection and feedback to the members of the rescue and treatment chain. The study includes cluster randomization of the participating hospitals.

Interventions

None listed

Sponsors

University Medical Center Goettingen
CollaboratorOTHER
St.Bernward Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patients after cardiac arrest

Exclusion criteria

* refused register participation by patient or legal representative

Design outcomes

Primary

MeasureTime frameDescription
In-hospital mortality3 weeksDeath/Survival at discharge

Secondary

MeasureTime frameDescription
CPC score3 weeksCerebral performance category
MRS3 weeksModified ranking scale

Countries

Germany

Contacts

Primary ContactKarl H Scholz, MD
k.scholz@fitt-stemi.de+4955139
Backup ContactThomas Meyer, MD
thomas.meyer@med.uni-goettingen.de+4955139

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026