The aim of the study is to evaluate the efficacy and safety of matrifen in patients with severe and chronic pain who can only be sufficiently treated with opioid analgesics (WHO class 3).
Study Type
OBSERVATIONAL
Enrollment
3,000
as defined in the Summary of Product Characteristics (Fachinformation Chapter 4.2)
Treatment success, efficacy of Matrifen
Time frame: within 1 month
Safety and tolerability of fentanyl and the transdermal system, quality of life
Time frame: within 1 month
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"Nycomed Deutschland GmbH"
Aachen, Germany
"Nycomed Deutschland GmbH"
Aalen, Germany
"Nycomed Deutschland GmbH"
Achim, Germany
"Nycomed Deutschland GmbH"
Ahaus, Germany
"Nycomed Deutschland GmbH"
Ahlen, Germany
"Nycomed Deutschland GmbH"
Aicha, Germany
"Nycomed Deutschland GmbH"
Albstadt, Germany
"Nycomed Deutschland GmbH"
Albstadt, Germany
"Nycomed Deutschland GmbH"
Alfeld, Germany
"Nycomed Deutschland GmbH"
Alfhausen, Germany
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