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Clinical Trial Summary

The primary objective of this study is to determine the variables associated with patient acceptation or refusal to participate in a clinical research protocol when seen in during a pneumology consultation (excluding oncology and tobaccology).


Clinical Trial Description

The secondary objectives of this study are:

- To compare patient acceptance rates for participation in a clinical research protocol before and after January 15, 2016.

- To determine the variables associated with accepting or refusing to participate in a clinical research protocol for patients seen during a pneumology consultation (excluding oncology and tobaccology) before January 15, 2016.

- To determine the variables associated with accepting or refusing to participate in a clinical research protocol for patients seen during a pneumology consultation (excluding oncology and tobaccology) after January 15, 2016.

- To describe the patient population seen during pneumology consultations.

- To determine the variables associated with accepting or refusing to participate in a clinical research protocol sponsored by a pharmaceutical laboratory.

- To determine the variables associated with accepting or refusing to participate in a clinical research protocol sponsored by an academic institution.

- Construct clusters (homogeneous groups) of patients seen during the pneumology consultations. ;


Study Design


Related Conditions & MeSH terms

  • Consulting in Pneumology Department, But Not for Oncology or Tobacology
  • Neoplasms

NCT number NCT03098303
Study type Observational
Source University Hospital, Montpellier
Contact
Status Completed
Phase
Start date December 23, 2014
Completion date December 13, 2016