Condition: Finger Injuries · Tendon Injury - Hand · Sponsor: University of Zurich
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.
This description comes directly from the study's public registry record.
Vera Beckmann-Fries · +41 44 255 51 24 · vera.beckmann-fries@usz.ch
Bernadette Tobler · +41 31 632 85 54 · bernadette.tobler@insel.ch
Always discuss trial participation with your own doctor first.
| University Hospital Zurich, Clinic of Reconstructive Surgery | Zurich, Canton of Zurich, Switzerland | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT04312412