A retrospective, observational study to investigate the therapeutic value of dexmedetomidine (dexdor®) in clinical practice (DexBOS)

08/07/2014
01/04/2024
EU PAS number:
EUPAS7037
Study
Finalised
Study type

Study topic

Human medicinal product

Study type

Non-interventional study

Scope of the study

Other

If ‘other’, further details on the scope of the study

Therapeutic use

Data collection methods

Secondary use of data
Non-interventional study

Non-interventional study design

Case-control
Population studied

Short description of the study population

Patients who have been treated with dexdor since it's introduction to the study sites.

Age groups

  • Adults (18 to < 46 years)
  • Adults (46 to < 65 years)
  • Adults (65 to < 75 years)
  • Adults (75 to < 85 years)
  • Adults (85 years and over)

Estimated number of subjects

200
Study design details

Main study objective

To investigate the therapeutic value of Dexdor in clinical practice in Belgium compared with matched control patients who received standard care.

Data analysis plan

To investigate the therapeutic value of Dexdor compared with matched historical controls.