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Outcome of the Treatment of Flexor Tendon Injuries

NCT04312412 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2021-12-13

No results posted yet for this study

Summary

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

  • Finger Injuries
  • Tendon Injury - Hand

Interventions

PROCEDURE

Controlled active motion (CAM)

Rehabilitation, post-surgery protocol

Sponsors & Collaborators

  • University Hospital, Basel, Switzerland

    collaborator OTHER

  • University of Bern

    collaborator OTHER

  • University of Zurich

    lead OTHER

Principal Investigators

  • Maurizio Calcagni, PD Dr. med. · University of Zurich

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-01-01
Primary Completion
2025-12-31
Completion
2026-12-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04312412 on ClinicalTrials.gov