Post-marketing Study to Collect Safety Data in Heart Transplant Patients Receiving Everolimus

NCT00134940 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2011-06-16

No results posted yet for this study

Summary

The purpose of this observational protocol is to evaluate the use of everolimus in routine clinical practice for heart transplants.

Primary outcome measures: incidence of acute rejection episodes Secondary outcomes: safety

Conditions

Sponsors & Collaborators

Principal Investigators

  • Novartis Pharmaceuticals · Novartis Pharmaceuticals

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-01-31
Primary Completion
2006-11-30
Completion
2006-11-30

Countries

  • Austria
  • Germany

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00134940 on ClinicalTrials.gov