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Recruiting NCT04312412

Outcome of the Treatment of Flexor Tendon Injuries

Observational Finger Injuries Tendon Injury - Hand

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Controlled active motion (CAM).
Who it may be relevant to
Registry conditions: Finger Injuries, Tendon Injury - Hand. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Switzerland
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Outcomes of Flexor Tendons Repair in Zones I-III From 2014-2025: a Swiss Multicenter Cohort Study

Overview

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.

Interventions

  • Procedure Controlled active motion (CAM)
    Rehabilitation, post-surgery protocol

Primary outcome measures

  • Range of motion [Time frame: 6 weeks]
  • Range of motion [Time frame: 13 weeks]
  • Range of motion [Time frame: 26 weeks]
  • Range of motion [Time frame: 52 weeks]
  • Grip or pinch strength [Time frame: 13 weeks]
  • Grip or pinch strength [Time frame: 26 weeks]
  • Grip or pinch strength [Time frame: 52 weeks]
  • Time return to work [Time frame: 52 weeks]

Eligibility criteria

Inclusion criteria

  • Injury between 2014 and 2025
  • Flexor tendon injury of the fingers or thumb in zones 1-3

Exclusion criteria

  • 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
  • Primary and secondary tendon reconstruction and tendon transfer

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

Switzerland · 1 center
  • University Hospital Zurich, Clinic of Reconstructive Surgery — Zurich

Publications

  • Beckmann-Fries V, Calcagni M, Schrepfer L, Kaempfen A, Vogelin E, Tobler-Ammann B. Relationship between pain, nerve injury and clinical outcomes after flexor tendon injuries in zones 1-2: a retrospective cohort study. Hand Ther. 2023 Jun;28(2):60-71. doi: 10.1177/17589983231159187. Epub 2023 Mar 29. PMID 37904861

Identifiers

NCT: NCT04312412 · BASEC-Nr. 2017-02267

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗