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A Retrospective, Medical Record Study to Investigate the Current Situation of Biopsy Testing in the Swedish Inoperable Non Small Cell Lung Cancer Patient Population


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Non Small Cell Lung Cancer

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Trial Information

A Retrospective, Medical Record Study to Investigate the Current Situation of Biopsy Testing in the Swedish Inoperable Non Small Cell Lung Cancer Patient Population


Inclusion Criteria:



- Diagnosis code C34 (ICD-10).

- Inoperable lung cancer.

- Diagnosis of lung cancer made between 2010-05-31 and 2009-06-01.

Exclusion Criteria:

- Diagnosis code C34.9b.

- Diagnosis code C34.9h.

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Retrospective

Outcome Measure:

Describe complications connected to biopsy and bronchoscopy in the investigated lung cancer population.

Outcome Time Frame:

Data will be collected retrospectively from medical records. Data of complications will be collected from when the complication occurred and then any overnight stay caused by complication, approximately a few days.

Safety Issue:

No

Principal Investigator

Dr Pål Falck, PhD

Investigator Role:

Study Director

Investigator Affiliation:

AstraZeneca

Authority:

Sweden: Regional Ethical Review Board

Study ID:

NIS-OSE-DUM-2010/1

NCT ID:

NCT01139619

Start Date:

October 2010

Completion Date:

January 2013

Related Keywords:

  • Non Small Cell Lung Cancer
  • Biopsy Mapping
  • Non small cell lung cancer
  • NSCLC
  • Lung cancer diagnosis
  • Retrospective
  • Inoperable Non Small Cell Lung Cancer
  • Carcinoma, Non-Small-Cell Lung
  • Lung Neoplasms

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