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Clinical Trials/NL-OMON38124
NL-OMON38124
Withdrawn
Not Applicable

A prospective randomised controlled study to evaluate ankle dorsiflexion after cast immobiliation and percutaneous gastrocnemius lengthening, for neurologic healthy children (6-18) with an symptomatic equinus contracture. - equinus contracture: cast vs percutaneous gastrocnemius lengthening.

Spaarne Ziekenhuis0 sites80 target enrollmentTBD
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Conditionsequinus contractureshort achilles tendon10028396

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
equinus contracture
Sponsor
Spaarne Ziekenhuis
Enrollment
80
Status
Withdrawn
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

Sponsor
Spaarne Ziekenhuis

Eligibility Criteria

Inclusion Criteria

  • •Patients (boys and girls) between 6\-18 years
  • •independent walking achieved
  • •symptomatic limited ankle dorsi flexion between \-10 and 3 degrees (with knee in extension and ankle in neutral position)
  • •patient has been treated non\-surgically for at least 6 month (NSAIDs, stretching, orthoses and physical therapy)
  • •Written informed consent both parents/ guardian (children 6\-12 years)
  • •written informed consent both parents/ guardian and child (children 12\-18 years)

Exclusion Criteria

  • •Patients with signs of neurological, orthopaedic or psychiatric disease.
  • •Patients with mental retardation
  • •Patients with previous surgery on the ankle
  • •Patients who were already treated with castimmobilisation because of equinus contracture
  • •Patients (12 years or older) whose parents are unable to understand informed consent
  • •Patients (12 years or older) or parents who are unable to fill out questionnaires
  • •Patients (12 years or older) or parents who are unable to understand treatment

Outcomes

Primary Outcomes

Not specified

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