Dose Adaptation of Capecitabine Using Mobile Phone Toxicity Monitoring

NCT01053104 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 26

Last updated 2012-07-25

No results posted yet for this study

Summary

To develop a system to manage side effects and adjust chemotherapy dose such that a patient can receive their personal maximum tolerated dose.

Conditions

Sponsors & Collaborators

  • oxBRC

    collaborator UNKNOWN
  • Vodafone UK Foundation

    collaborator UNKNOWN
  • Centre for Statistics in Medicine

    collaborator OTHER
  • Oncology Clinical Trials Office (OCTO, Oxford)

    collaborator UNKNOWN
  • University of Oxford

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2010-12-31
Completion
2011-04-30

Countries

  • United Kingdom

Study Locations

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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 NCT01053104 on ClinicalTrials.gov