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Dapagliflozin in patients with Right Heart Failure (Dapa-RHF)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-515044-23-01
Acronym
2021-01755
Enrollment
30
Registered
2024-08-30
Start date
2024-04-29
Completion date
Unknown
Last updated
2024-08-30

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

Conditions

Chronic right heart failure

Brief summary

Change in serum NT-proBNP level from baseline to end of treatment (Delta-NTproBNP)

Detailed description

Change in quality of life assessed by overall summary score of the Kansas City Cardiomyopathy Questionnaire (KCCQ) (a specific HF patient reported outcome questionnaire) from baseline to end of treatment, Change in RV ejection fraction (RV EF) [%] assessed in cardiac MRI from baseline to end of treatment, Change in exercise capacity assessed by the 6 min walking distance [meters] from baseline to end of treatment, Change in NYHA (New York Heart Association) class from baseline to end of treatment

Interventions

DRUGDapagliflozin Placebo tablets
DRUGDAPAGLIFLOZIN

Sponsors

Universitaetsmedizin Goettingen
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Change in serum NT-proBNP level from baseline to end of treatment (Delta-NTproBNP)

Secondary

MeasureTime frame
Change in quality of life assessed by overall summary score of the Kansas City Cardiomyopathy Questionnaire (KCCQ) (a specific HF patient reported outcome questionnaire) from baseline to end of treatment, Change in RV ejection fraction (RV EF) [%] assessed in cardiac MRI from baseline to end of treatment, Change in exercise capacity assessed by the 6 min walking distance [meters] from baseline to end of treatment, Change in NYHA (New York Heart Association) class from baseline to end of treatment

Countries

Germany

Outcome results

None listed

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