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Clinical Trials/DRKS00005175
DRKS00005175
Completed
Phase 1

Evaluation of the reconstruction osteochondrale lesions of the talus. - Talus-Study

niversität Würzburg Orthopädische Klinik0 sites67 target enrollmentJanuary 3, 2014

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Osteochonrale lesions of the talus.
Sponsor
niversität Würzburg Orthopädische Klinik
Enrollment
67
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 3, 2014
End Date
June 30, 2017
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversität Würzburg Orthopädische Klinik

Eligibility Criteria

Inclusion Criteria

  • osteochndrale lesions of the talus in phase 3 (2\) and 4 according to Berndt and Harty with areal damage sizes of 1,5 cm2
  • \-faultless proximity cartilage and bordering hintfoot bones

Exclusion Criteria

  • Patients who not fulfill all inclution criteria
  • \- drug or other addiction
  • \- women during pregnancy or during breast feeding
  • \- patients incapable of contracting
  • \- patients with compulsory treatment
  • \- psychological diseases with reduced compliance,
  • \- chronical diseases of infection
  • \- autoimmune diseases
  • \- extra risk of bleeding
  • \- metabolic arthritis (i.e. gout, pseudo gout)

Outcomes

Primary Outcomes

Not specified

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