Study to Evaluate the Safety of Twice Daily Oral Carvedilol

Update Il y a 4 ans
Reference: NCT00129363

Woman and Man

Extract

The objective of this study is to evaluate the long-term safety of carvedilol in pediatric patients with chronic heart failure, who completed the Pediatric Carvedilol Study 321. Carvedilol will be provided as open-label therapy for a period of at least 6 months (or until termination of the study) by SmithKline Beecham Corporation d/b/a GlaxoSmithKline (GSK) or the University Sponsor.


Inclusion criteria

  • Congestive heart failure

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