Assessment of Complications, Quality of Life and Easiness of Use of Implantable Central Venous Access Ports

NCT00921141 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 815

Last updated 2012-07-23

No results posted yet for this study

Summary

This is a prospective, descriptive and observational study of the anticancer center practice

Conditions

Sponsors & Collaborators

  • Centre Oscar Lambret

    lead OTHER

Principal Investigators

  • Fabrice NARDUCCI, MD · Centre Oscar Lambret

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-05-31
Primary Completion
2007-04-30
Completion
2009-04-30

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

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 NCT00921141 on ClinicalTrials.gov