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Clinical Trial Summary

Evaluation of patient reported outcomes (PRO) with tumor cachexia in a real life setting.


Clinical Trial Description

The PRO Xie project will recruit a representative cohort of patients with advanced lung or advanced pancreatic cancer with a high risk for the development of cancer cachexia.

Patient Reported Outcomes (PRO) are assessed in a real life setting by a questionnaire consisting of 20 questions: QoL is measured by SF12, fatigue by FACIT-F and cachexia by FAACT questionnaires, respectively.

These data will determine the potential need for anti-cachexia treatment in those patients, as well as the number of underweight patients, the evaluation of general QoL, fatigue and cachexia and the evaluation of malnutrition. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02983500
Study type Observational
Source iOMEDICO AG
Contact
Status Completed
Phase
Start date August 28, 2016
Completion date July 24, 2019

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