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OpenTrials
Completed

NCT Number: NCT00211601

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Disease Management Assessment

Behavioral

Primary outcomes

  1. CINV at the delayed phase during cycle 2

Secondary outcomes

  1. Treatment for CINV

Sponsors and collaborators

Lead sponsor

Merck Sharp & Dohme LLC

Industry

Registry information

Official study title

Study of Chemotherapy and Patient Health Outcomes for Nausea and Emesis

Acronym: C-PHONE

Important dates

Study start
2004
Primary completion
2005
Study completion
2005
First posted
Sep 21, 2005
Registry last updated
May 1, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.