Skip to main content
OpenTrials
Completed

NCT Number: NCT01999621

Determinants of Intensity of Care of Lung Cancer Patients With Organ Failure

Investigators will evaluate determinants of the patients' care type : palliative, medical or intensive care. The place of patient or family on care's decision will be noticed. Investigators will evaluate 3 month-survival and patients' feelings (visit with a psychologist) according to type of care they benefited.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Lung Cancer Lung Diseases Lung Neoplasms Neoplasms Neoplasms by Site Respiratory Tract Diseases Respiratory Tract Neoplasms Thoracic Neoplasms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital of Grenoble

Grenoble, 38043, France

About this study

Two hundred patients have to be enrolled in 2 years in the Grenoble Teaching Hospital and in the Saint Louis hospital in Paris between November 2010 and November 2012. Each lung cancer patient with at least one organ failure, admitted in emergency, thoracic oncology or directly in ICU will be included.

The objectives are to identify patients' characteristics associated with proposition for intensive care unit admission and those associated with the decision of intensive care unit admission.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • lung cancer
  • Organ failure

Exclusion criteria

-

Treatment and study plan

Primary outcomes

  1. Identify an association between patients' characteristics and proposition for intensive care unit admission.

    Time frame: at day 0

    univariate and multivariate logistic regression

Secondary outcomes

  1. Identify an association between patients' characteristics and decision of intensive care unit admission among patients proposed for ICU admission

    Time frame: at day 0

    univariate and multivariate logistic regression

Other outcomes

  1. identify patients' characteristics associated with survival

    Time frame: up to 4 months after the last inclusion

    Cox' model

  2. patients' feelings according to intensity of care they received

    Time frame: at 3 months

    hospital anxiety and depression scale, SF-36 scale and Impact of Event Scale-R and a visit with a psychologist

Sponsors and collaborators

Lead sponsor

University Hospital, Grenoble

Other

Registry information

Acronym: CBP-DO

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Dec 3, 2013
Registry last updated
Dec 3, 2013

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.

Related clinical trials

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