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Collaborative Systematic Overview of Randomised Controlled Trials of Beta-Blockers in the Treatment of Heart Failure

Collaborative Systematic Overview of Randomised Controlled Trials of Beta-Blockers in the Treatment of Heart Failure

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00832442
Acronym
BB-META-HF
Enrollment
18240
Registered
2009-01-30
Start date
2008-08-31
Completion date
2012-12-31
Last updated
2012-05-09

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

Conditions

Heart Failure

Keywords

Beta blocker, Heart Failure, Meta analysis, Individual patient data

Brief summary

Several large trials have shown that beta-blocker treatment reduces the risk of death and hospital admission in patients with symptomatic heart failure. Unfortunately, survey data suggests relatively poor utilisation of beta-blockers, despite ample evidence for good tolerability. Additionally there are several important unanswered questions, such as clinical efficacy for specific sub-populations (women, the elderly and patients with diabetes or other co-morbidities) and the effect of beta-blockers in combination with other medications. Previous meta-analyses, based on published tabular data, have been conducted although this approach has important biases and limitations. We plan to perform a carefully conducted systematic review of individual patient data from the major randomised trials of beta-blockers in heart failure. The goals of this collaborative project are to clarify the overall efficacy of beta-blockers and identify sub-groups that show particular benefit, thereby increasing the use of beta-blockers, reducing adverse clinical outcomes and the high costs associated with this condition.

Interventions

DRUGBeta blocker

as determined by individual study

OTHERPlacebo

in addition to usual care

Sponsors

University of Oxford
CollaboratorOTHER
Royal Brompton & Harefield NHS Foundation Trust
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Randomised control trials of beta-blocker versus control in patients with documented heart failure * Unconfounded trials only (in which one treatment group differed from another only by the beta-blocker therapy of interest) * Randomization process precluded prior knowledge of the next treatment (for example trials in which treatment allocation was alternate or based on odd or even dates would not be included)

Exclusion criteria

* Trial sample size of less than 300 patients

Design outcomes

Primary

MeasureTime frame
Beta-blocker therapy improves overall mortality and morbidity in symptomatic heart failure in an individual patient meta-analysisvariable (time to event)

Secondary

MeasureTime frame
Beta-blocker therapy improves mortality and morbidity in patients with co-morbidities (diabetes, renal dysfunction, COPD, peripheral arterial disease or atrial fibrillation)variable (time to event)
The benefit of beta-blockers is not modified by concomitant cardiovascular therapyvariable (time to event)
Beta-blocker therapy improves mortality and morbidity in both elderly patients and womenvariable (time to event)
The clinical benefit is dependent on the resting heart rate achieved whatever the dose achieved or agent usedvariable (time to event)
Adverse side effects of beta blocker therapy do not significantly impact on clinical benefit (as a whole and in relevant sub-groups)variable (time to event)
The benefit of beta-blockers is independent of left ventricular ejection fraction at baselinevariable (time to event)

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026