Study of Chemotherapy and Patient Health Outcomes for Nausea and Emesis (0000-041) (C-PHONE)

This study has been completed.
Information provided by (Responsible Party):
Merck Sharp & Dohme Corp. Identifier:
First received: September 13, 2005
Last updated: May 2, 2014
Last verified: May 2014

The purpose of this study is to assess whether timely feedback to providers on patient experiences with delayed chemotherapy induced nausea and vomiting (CINV) lead to differences in patient outcomes for subsequent cycles.

Condition Intervention
Chemotherapy Induced Nausea and Vomiting
Behavioral: Disease Management Assessment

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Official Title: Study of Chemotherapy and Patient Health Outcomes for Nausea and Emesis

Resource links provided by NLM:

Further study details as provided by Merck Sharp & Dohme Corp.:

Primary Outcome Measures:
  • CINV at the delayed phase during cycle 2

Secondary Outcome Measures:
  • Treatment for CINV

Estimated Enrollment: 1500
Study Start Date: August 2004
Study Completion Date: December 2005

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Highly or moderately emetogenic chemotherapy planned for at least 2 cycles

Exclusion Criteria:

  • Concurrent other anti-cancer therapy (e.g. radiation, hormone, etc.); vomiting during the 24 hours prior to first chemotherapy cycle; having a disease/condition or taking medication that may cause emesis
  Contacts and Locations
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Please refer to this study by its identifier: NCT00211601

Sponsors and Collaborators
Merck Sharp & Dohme Corp.
Study Director: Medical Monitor Merck Sharp & Dohme Corp.
  More Information

No publications provided

Responsible Party: Merck Sharp & Dohme Corp. Identifier: NCT00211601     History of Changes
Other Study ID Numbers: 0000-041, 041, 2005_072
Study First Received: September 13, 2005
Last Updated: May 2, 2014
Health Authority: United States: Food and Drug Administration processed this record on March 31, 2015