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Educational Intervention to Adherence of Patients Treated by Capecitabine +/- Lapatinib

NCT01847599 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 65

Last updated 2017-07-21

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy of the implementation of an educational program on adherence to capecitabine alone or in combination to lapatinib.

Conditions

Interventions

OTHER

Educational Intervention to enhance the adherence of Patient treated by capecitabine +/- Lapatinib

Sponsors & Collaborators

  • Centre Jean Perrin

    lead OTHER

Principal Investigators

  • Isabelle VAN PRAAGH, MD · Centre Jean Perrin

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-09-06
Primary Completion
2016-10-13
Completion
2017-07-02

Countries

  • France

Study Locations

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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 NCT01847599 on ClinicalTrials.gov