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Clinical Trials/NL-OMON51193
NL-OMON51193
Recruiting
N/A

Function and participation of children with Ponseti treated clubfoot - Function and Participation of clubfootpatients

Maxima Medisch Centrum0 sites90 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Maxima Medisch Centrum
Enrollment
90
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Maxima Medisch Centrum

Eligibility Criteria

Inclusion Criteria

  • Both controls and (relapse) clubfoot patients who:
  • \- Are 5 \- 9 years old
  • \- Have parents with sufficient command of the Dutch language
  • Clubfoot patients who:
  • \- Have idiopathic clubfoot
  • \- Are uni\- or bilaterally affected
  • \- Have been primarily treated with the Ponseti method
  • Relapse clubfoot patients:
  • \- Reoccurrence of one or more clubfoot aspects that requires additional
  • treatment as judged by the expert opinion of the treating orthopaedic surgeon.

Exclusion Criteria

  • Both controls and (relapse) clubfoot patients who:
  • \- Are unable to follow the instructions
  • \- Have obesity, based on their age\-category and gender
  • \- Have an underlying syndrome
  • \- Have a neurological disease
  • Controls who:
  • \- Have problems of the lower extremity
  • (e.g., hip dysplasia/ broken leg \<1year prior to participation)
  • All clubfoot patients who:
  • Did not have their primary treatment in the Netherlands

Outcomes

Primary Outcomes

Not specified

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