Effectiveness and Safety of OSTENIL® TENDON in the Treatment of Pain and Restricted Mobility in Tendon Disorders

ConditionTendinopathy
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-99
SponsorTRB Chemedica AG

About this trial

PMCF study to further substantiate the effectiveness and safety of OSTENIL® TENDON in the overall as well as indication-specific treatment of pain and restricted mobility in four different tendon disorders (patella tendon, peroneal tendon, medial epicondylus humeri and iliotibial band) in a real-life clinical setting when used according to the instructions for use.

Eligibility criteria

Qualifiers

Patient aged between 18 and 99 years

Diagnosis of symptomatic tendinopathy (patella tendon, peroneal tendon, medial epicondylus humeri or iliotibial band)

Physician's recommendation to use OSTENIL® TENDON prior to recruitment

Signed informed consent

Disqualifiers

Presence of any contra-indication or precautionary condition listed in the instructions for use, i.e.,

Ascertained hypersensitivity to any of the OSTENIL® TENDON constituents

Known pregnancy or breast feeding

Acute trauma

Trial design

Treatments tested in this trial

  • OSTENIL® TENDON

Treatment groups

84 Participants
are divided into 1 treatment group

Sponsors and collaborators