- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00470756
Forefoot Adduction (FFA) in Infants and Toddlers. Differences of Neuromuscular Activity.
Difference of Neuromuscular Activity in Infants and Toddlers With Foot Dorsiflexion Compare to Infants and Toddlers With Foot Plantarflexion
Every week we encounter with 5-8 pairs of worried parents of infants with forefoot adduction. Most of them usually need only reassurance and education how to manipulate the deformed foot. During the examination we usually use provocative maneuver to trigger peroneal activity. This manual stimulation usually reveals active eversion and dorsiflexion of the foot in most of the children, but not in all of them. Small part of the children reacts in opposite direction - instead of the typical eversion they demonstrate inversion and some plantar flexion of the foot. We have the impression that this subgroup of children improves the deformity slower and sometime less complete than most of the children. We did not find in the literature any description of this phenomenon. We postulate, that atypically reacting patients probably have different response due to abnormalities of neuromuscular balance between invertors-flexors and evertors-extensors muscle groups. This small subgroup of children may need more close follow-up and probably casting to speed up and secure the improvement of their deformity.
Study goals:
Evaluate ability of children with FFA to respond on mechanical triggering of peroneal activity
- The majority of the patients with standard reaction - foot dorsiflexion and eversion (evertors)
- The minority of the patients with nonstandard reaction - foot plantarflexion and inversion (invertors)
- Evaluate randomly selected children from each group for character of muscular response on electrical stimulation (EMG) of calf muscles.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
-
Jerusalem, Israel
- Hadassah Medical Organization.
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Boys and girls between two months and one year old.
- Non associated pathology.
- Signing Informed consent.
Exclusion Criteria:
- Unwillingness to sign informed consent.
- Associated pathology
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
evertors, invertors
|
mechanical triggering of peroneal activity
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Naum Simanovski, MD, Hadassah Medical Organization
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- SIM03-HMO-CTILL
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