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"Comparison between norepinephrine and dobutamine in patients with cardiogenic shock"

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-520399-84-00
Enrollment
46
Registered
2025-02-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-11

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

Conditions

Cardiogenic shock

Brief summary

- Change in blood lactate concentration measured as the difference between the maximum value at baseline: 0-1 hours after randomization and 72 hours after randomization, in the two treatment arms. - In case of death: change in blood lactate concentration measured as the difference between the maximum value at baseline: 0-1h after randomization and the last available lactate value from randomization, in the two treatment arms.

Detailed description

- death or need for ECMO/LVAD at 72 hours - death or need for ECMO/LVAD at discharge - change in SOFA score between baseline (0-1 hour from randomization) and 72 hours from randomization and between baseline (0-1 hour from randomization) and 7 days from randomization - lactate AUC (0-72 hours) - need for additional extra-trial inotrope at 72 hours

Interventions

DRUGDOBUTAMINE

Sponsors

Azienda Unita' Sanitaria Locale Toscana Sud Est
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
- Change in blood lactate concentration measured as the difference between the maximum value at baseline: 0-1 hours after randomization and 72 hours after randomization, in the two treatment arms. - In case of death: change in blood lactate concentration measured as the difference between the maximum value at baseline: 0-1h after randomization and the last available lactate value from randomization, in the two treatment arms.

Secondary

MeasureTime frame
- death or need for ECMO/LVAD at 72 hours - death or need for ECMO/LVAD at discharge - change in SOFA score between baseline (0-1 hour from randomization) and 72 hours from randomization and between baseline (0-1 hour from randomization) and 7 days from randomization - lactate AUC (0-72 hours) - need for additional extra-trial inotrope at 72 hours

Countries

Italy

Outcome results

None listed

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