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Comparative Effects of Nebivolol and Carvedilol on Diastolic Function in the Elderly Heart Failure Patients

Comparative Effects of Nebivolol and Carvedilol on Diastolic Function of the Left Ventricle in the Elderly Heart Failure Patients With Preserved Ejection Fraction: Study Protocol for a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02619526
Enrollment
62
Registered
2015-12-02
Start date
2016-12-31
Completion date
2018-12-31
Last updated
2018-02-05

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

Conditions

Heart Failure

Brief summary

Heart failure (HF) is a common and disabling condition in the elderly. Randomized clinical trials and meta-analyses have clearly demonstrated that long-term use of β blockers improves the outcomes of patients with HF. However, limited data have been available on the treatment of HF with preserved ejection fraction (EF) in the elderly. No study has specifically compared the relative effectiveness of carvedilol and nebivolol in treating HF in old age patients with preserved EF.

Detailed description

This trial is a prospective, randomized, open-label, active controlled study designed to investigate effects of nebivolol and carvedilol on diastolic function of the left ventricle (LV) in the elderly HF patients with preserved EF. Patients will be included in the study if they had LVEF ≥ 40%, NYHA functional class I, II or III, and clinical stability without hospital admission for HF in the preceding 3 months.

Interventions

DRUGNebivolol

Nebivolol 10mg, once a day

DRUGCarvedilol

Carvedilol 25mg, twice a day

Sponsors

Menarini Group
CollaboratorINDUSTRY
Dong-A University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
70 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* more than 70 years * EF ≥ 40%

Exclusion criteria

* contraindication to the study drug

Design outcomes

Primary

MeasureTime frame
the ratio of transmitral E velocity to early diastolic mitral annular velocity (E/E')12 months

Countries

South Korea

Contacts

Primary ContactYieun-Ji Lee, RN
oneday140412@naver.com82-51-240-2959

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026