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Clinical Trial Summary

There is a lack of knowledge among patients concerning their treatment with bDMARDs, which could lead to low adherence.

The objective of this study is to assess the impact of a pharmacist's intervention on the adherence to bDMARDs in patients with Spondyloarthritis.


Clinical Trial Description

This is an interventional, controlled, open-label and monocentric study. 80 patients are planned to be included.

After written informed consent will be obtained, the patients will be randomized in two arms:

- Intervention arm: intervention of a pharmacist who will explain bDMARDs management.

- Control arm, without intervention.

Two primary end-points are defined:

1. the changes from baseline to M6 in the patients' knowledge score about subcutaneous bDMARD management

2. the changes from baseline to M6 in Medication Possession Ratio (MPR)

As secondary end-points, the changes in disease activity and patients' satisfaction regarding the pharmacists' intervention are evaluated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04001673
Study type Interventional
Source Hôpital Cochin
Contact
Status Completed
Phase N/A
Start date February 15, 2017
Completion date September 15, 2018

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