Actively Recruiting
Outcome of the Treatment of Flexor Tendon Injuries
Led by University of Zurich · Updated on 2021-12-13
500
Participants Needed
1
Research Sites
678 weeks
Total Duration
On this page
Sponsors
U
University of Zurich
Lead Sponsor
U
University Hospital, Basel, Switzerland
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Outcome of the Treatment of Flexor Tendon Injuries
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Injury between 2014 and 2025
- Flexor tendon injury of the fingers or thumb in zones 1-3
You will not qualify if you...
- No given consent
- Concomitant injuries such as fractures, large soft tissue injuries, or replantation
- Bony avulsion fracture of flexor tendon (Jersey finger)
- Basic diseases such as rheumatoid diseases
- Primary and secondary tendon reconstruction and tendon transfer
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospital Zurich, Clinic of Reconstructive Surgery
Zurich, Canton of Zurich, Switzerland, 8091
Actively Recruiting
Research Team
V
Vera Beckmann-Fries
CONTACT
B
Bernadette Tobler
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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