Skip to content

DANOHCA: The Danish Out-of-Hospital Cardiac Arrest study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-515997-28-00
Acronym
DANOHCA-001
Enrollment
1000
Registered
2024-10-11
Start date
2023-06-16
Completion date
Unknown
Last updated
2025-12-05

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

Conditions

Patients resuscitated from out-of-hospital cardiac arrest

Brief summary

The protective effect of dexamethasone decided by all-cause mortality at 90 days following cardiac arrest, The protective effect of elevated backrest (30-45 degrees) decided by all-cause mortality at 90 days following cardiac arrest, The protective effect of early wake up and extubation ≤6 hours after admission decided by days alive outside hospital within 30 days, The protective effect of olanzapine decided by days alive outside hospital within 30 days

Detailed description

All-cause mortality at 90 days (in study strata where it is not a primary endpoint), Serum Neuron Specific Enolase and Light Chain Neurofilament levels at 48h, Markers of organ damage other than CNS: 1) TNT or TNI and CKMB (cardiac) and proBNP during initial 72h and 2) Creatinine during initial 72h and the use of dialysis during the first 30 days post OHCA (renal), Need for vasopressor during ICU stay. (cumulative doses during the first 36 hours and total doses), Mixed blood venous saturation after 12, 24 and 36 hours and the daily during ICU stay, Duration of intubation (oral and tracheostomy combined), Number of unconscious patients at 96 hours, Number of CAM-ICU positive patients 24 hours after extubation, Number of CAM-ICU negative days, Number of days without pharmacological treatment for delirium (other than study drug during the intervention period), ICU length of stay, Hospital length of stay (including in-patient rehabilitation and transfer to referral hospital), CPC and mRS at ICU discharge, at hospital discharge and at 90 days

Interventions

DRUGPLACEBO
DRUGZYPREXA VELOTAB 10 mg orodispersible tablets
DRUGopløsning

Sponsors

Rigshospitalet
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The protective effect of dexamethasone decided by all-cause mortality at 90 days following cardiac arrest, The protective effect of elevated backrest (30-45 degrees) decided by all-cause mortality at 90 days following cardiac arrest, The protective effect of early wake up and extubation ≤6 hours after admission decided by days alive outside hospital within 30 days, The protective effect of olanzapine decided by days alive outside hospital within 30 days

Secondary

MeasureTime frame
All-cause mortality at 90 days (in study strata where it is not a primary endpoint), Serum Neuron Specific Enolase and Light Chain Neurofilament levels at 48h, Markers of organ damage other than CNS: 1) TNT or TNI and CKMB (cardiac) and proBNP during initial 72h and 2) Creatinine during initial 72h and the use of dialysis during the first 30 days post OHCA (renal), Need for vasopressor during ICU stay. (cumulative doses during the first 36 hours and total doses), Mixed blood venous saturation after 12, 24 and 36 hours and the daily during ICU stay, Duration of intubation (oral and tracheostomy combined), Number of unconscious patients at 96 hours, Number of CAM-ICU positive patients 24 hours after extubation, Number of CAM-ICU negative days, Number of days without pharmacological treatment for delirium (other than study drug during the intervention period), ICU length of stay, Hospital length of stay (including in-patient rehabilitation and transfer to referral hospital), CPC and mRS a

Countries

Denmark

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026