MedPath

Beta-blockade in cardiac arrest

Phase 2
Recruiting
Conditions
cardiac arrest, ventricular fibrillation
Registration Number
2024-518949-14-00
Lead Sponsor
Medical University Of Vienna
Brief Summary

To demonstrate that add-on treatment with landiolol in patients

with cardiac arrest significantly decreases the time to sustained

ROSC (sROSC) (time from infusion of study medication to sustained

ROSC)

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing, recruiting
Sex
Not specified
Target Recruitment
48
Inclusion Criteria

OHCA , ³ 18 years of age • 3 or more shockable rhythms (VF or pVT) and last rhythm shockable

Exclusion Criteria

Age > 85a • Severe head trauma or acute active bleeding • Known allergy or insensitivity to landiolol or another b-blocker

Study & Design

Study Type
Not specified
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time (in minutes) to sustained return of spontaneous circulation

Time (in minutes) to sustained return of spontaneous circulation

Secondary Outcome Measures
NameTimeMethod
cummulative ROSC, temporary ROSC, sustained ROSC, survival at 24h, favorable neurologic outcome

cummulative ROSC, temporary ROSC, sustained ROSC, survival at 24h, favorable neurologic outcome

Trial Locations

Locations (1)

Medical University Of Vienna

🇦🇹

Vienna, Austria

Medical University Of Vienna
🇦🇹Vienna, Austria
Michael Holzer
Site contact
+4314040029810
michael.holzer@meduniwien.ac.at

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