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DECISION; Digoxin Evaluation in Chronic heart failure: Investigational Study In Outpatients in the Netherlands

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-509898-23-00
Enrollment
982
Registered
2024-10-18
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

heart failure

Brief summary

The primary endpoint is the composite of (repeated) HF hospitalizations, (repeated) urgent HF hospital visits and cardiovascular death.

Detailed description

All-cause mortality, Cardiovascular death., (Repeated) HF hospitalization, (repeated) urgent HF hospital visits, Cost-effectiveness., All-cause hospitalizations., Unscheduled cardiovascular hospital visits., Days alive out of hospital., Quality of Life., Heart rate in both AF and sinus rhythm., To assess side effects (including SUSARs) associated with study medication., Initiation of (recurrence of) AF in patients with sinus rhythm at baseline., Conversion to sinus rhythm and maintenance of sinus rhythm in patients with AF at baseline, Proteomics and validating hits in elisa's

Interventions

DRUGDIGOXIN

Sponsors

Universitair Medisch Centrum Groningen
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the composite of (repeated) HF hospitalizations, (repeated) urgent HF hospital visits and cardiovascular death.

Secondary

MeasureTime frame
All-cause mortality, Cardiovascular death., (Repeated) HF hospitalization, (repeated) urgent HF hospital visits, Cost-effectiveness., All-cause hospitalizations., Unscheduled cardiovascular hospital visits., Days alive out of hospital., Quality of Life., Heart rate in both AF and sinus rhythm., To assess side effects (including SUSARs) associated with study medication., Initiation of (recurrence of) AF in patients with sinus rhythm at baseline., Conversion to sinus rhythm and maintenance of sinus rhythm in patients with AF at baseline, Proteomics and validating hits in elisa's

Countries

Netherlands

Outcome results

None listed

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