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Patient Reported Outcomes Registry in Patient With Cancer Cachexia (PROXie)

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iOMEDICO

Status

Completed

Conditions

Metastatic Pancreatic Cancer
NSCLC, Metastatic

Study type

Observational

Funder types

Industry

Identifiers

NCT02983500
IOM-0050346

Details and patient eligibility

About

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

Full 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.

Enrollment

253 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Documented diagnosis of NSCLC UICC stage IIIB/IV or pancreatic cancer UICC stage III/IV
  • Start of the first line palliative systemic treatment
  • Ability to read and understand German
  • Written informed consent

Exclusion criteria

  • None

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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