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Clinical Trial Summary

The purpose of this study is to determine the prevalence of breakthrough cancer pain and characterize breakthrough cancer pain in an unselected, representative cohort of cancer outpatients with or without pain who attend consultations.


Clinical Trial Description

This study has been designed as a non-interventional, non post-authorization, cross-sectional, epidemiological study to determine the prevalence of breakthrough cancer pain and characterize breakthrough cancer pain in an non-selected, representative cohort of cancer outpatients with or without pain.

The study enrolled 3765 patients. This multicenter trial will be conducted in Spain. Data from participants will be collected through questionnaire and medical history in a single visit (up to 1 month). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02899884
Study type Observational
Source Takeda
Contact
Status Completed
Phase
Start date November 14, 2016
Completion date July 16, 2018

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