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Clinical Trials/NL-OMON31898
NL-OMON31898
Completed
Not Applicable

A pilot randomized controlled trial comparing the effect of a percutaneous and lipofilling technique in patients with a primary Dupuytren*s contracture with standard fasciectomy surgery on convalescence, contracture correction and recurrence rate. - RCT comparing two surgical techniques for Dupuytren's contracture

Erasmus MC, Universitair Medisch Centrum Rotterdam0 sites80 target enrollmentTBD
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ConditionsDupuytren's contracturehand diseases1001076110040795

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dupuytren's contracture
Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Enrollment
80
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •\- males and females
  • •\- all ages
  • •\- primary Dupuytren\*s contracture
  • •\- PIP \> 30º/ MCP \> 20º
  • •\- one or more affected rays
  • •\- severe or less severe diatheses
  • •\- American society of Anaesthesiologists (ASA) criteria I, II and III

Exclusion Criteria

  • •\- recurrent Dupuytren\*s contracture
  • •\- history of hand surgery on the affected finger(s)
  • •\- use of blood thinners that can not be stopped for surgery
  • •\- ASA IV and V

Outcomes

Primary Outcomes

Not specified

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