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A Study to Evaluate Corrected QT Interval From Clinical Studies Conducted With Bevacizumab

Withdrawn
Conditions
Carcinoma
Registration Number
NCT00477425
Lead Sponsor
Genentech, Inc.
Brief Summary

This is a supplemental study designed to evaluate the effect of bevacizumab on QTc interval in cancer patients. Patients who have consented to participate in selected randomized controlled bevacizumab clinical trials will be invited to participate in this study.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Signed Informed Consent Form
  • Enrollment in one of a list of certain randomized, controlled bevacizumab trials
Exclusion Criteria
  • Implantable pacemaker or automatic implantable cardioverter defibrillator (AICD)
  • Congenital long QT syndrome
  • Family history of long QT syndrome
  • Clinically significant bradycardia (defined as < 50 beats/minute)

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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