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

Lung Cancer Clinical Trial

— CBP-DO  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01999621
• Other study ID #: 2010-16
• Status: Completed
• Phase: N/A
• First received: October 15, 2013
• Last updated: November 25, 2013
• Start date: December 2010
• Est. completion date: November 2012

Study information

• Verified date: November 2013
• Source: University Hospital, Grenoble
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Institutional Ethical CommitteeFrance: The Commission nationale de l’informatique et des libertés
• Study type: Observational

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 140
• Est. completion date: November 2012
• Est. primary completion date: November 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• lung cancer

• Organ failure

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Lung Cancer
• Lung Neoplasms

Locations

Country	Name	City	State
France	University Hospital of Grenoble	Grenoble

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	identify patients' characteristics associated with survival	Cox' model	up to 4 months after the last inclusion	No
Other	patients' feelings according to intensity of care they received	hospital anxiety and depression scale, SF-36 scale and Impact of Event Scale-R and a visit with a psychologist	at 3 months	No
Primary	Identify an association between patients' characteristics and proposition for intensive care unit admission.	univariate and multivariate logistic regression	at day 0	No
Secondary	Identify an association between patients' characteristics and decision of intensive care unit admission among patients proposed for ICU admission	univariate and multivariate logistic regression	at day 0	No