Outcome of the Treatment of Flexor Tendon Injuries
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorUniversity of Zurich
About this trial
In order to gather enough data for meaningful statistics, a multicenter register of all flexor tendon repairs was established with surgical, clinical and rehabilitation patient data. The controlled active motion (CAM) protocol was administered in all patients after surgery. The purpose was to (i) measure surgery and therapy outcomes in the three centers and (ii) evaluate potential influencing factors on outcomes.
Eligibility criteria
Qualifiers
Injury between 2014 and 2025
Flexor tendon injury of the fingers or thumb in zones 1-3
Disqualifiers
No given consent
Concomitant injuries as fractures, large soft tissue injuries, replantation
Bony avulsion fracture of flexor tendon (Jersey finger)
Basic disease as rheumatoid diseases
Trial design
Treatments tested in this trial
- Controlled active motion (CAM)
Treatment groups
No treatment groups listed
Sponsors and collaborators
University of Zurich
Lead sponsor
University Hospital, Basel, Switzerland
Collaborator
University of Bern
Collaborator
Source ClinicalTrials.gov