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Forefoot Adduction (FFA) in Infants and Toddlers. Differences of Neuromuscular Activity.
This study is currently recruiting participants.
Verified by Hadassah Medical Organization, November 2008
Sponsored by: Hadassah Medical Organization
Information provided by: Hadassah Medical Organization
ClinicalTrials.gov Identifier: NCT00470756
  Purpose

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:

  1. Evaluate ability of children with FFA to respond on mechanical triggering of peroneal activity

    1. The majority of the patients with standard reaction - foot dorsiflexion and eversion (evertors)
    2. The minority of the patients with nonstandard reaction - foot plantarflexion and inversion (invertors)
  2. Evaluate randomly selected children from each group for character of muscular response on electrical stimulation (EMG) of calf muscles.

Condition Phase
Forefoot Adduction
Phase II

MedlinePlus related topics: Foot Health
U.S. FDA Resources
Study Type: Observational
Study Design: Prospective
Official Title: Difference of Neuromuscular Activity in Infants and Toddlers With Foot Dorsiflexion Compare to Infants and Toddlers With Foot Plantarflexion

Further study details as provided by Hadassah Medical Organization:

Estimated Enrollment: 20
Study Start Date: March 2008
Estimated Primary Completion Date: March 2009 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   2 Months to 1 Year
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Boys and girls between two months and one year old.
  2. Non associated pathology.
  3. Signing Informed consent.

Exclusion Criteria:

  1. Unwillingness to sign informed consent.
  2. Associated pathology
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00470756

Contacts
Contact: Naum Simanovski, MD 0097226776292 siman303@zahav.net.il
Contact: Hadas Lemberg, PhD 2 6777572 ext 00 972 lhadas@hadassah.org.il

Locations
Israel
Hadassah Medical Organization. Recruiting
Jerusalem, Israel
Contact: Arik Tzukert     00 972 2 6776095     arik@hadassah.org.il    
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Principal Investigator: Naum Simanovski, MD : Hadassah Medical Organization, Jerusalem, Israel
  More Information

No publications provided

Study ID Numbers: SIM03-HMO-CTILL
Study First Received: May 6, 2007
Last Updated: November 5, 2008
ClinicalTrials.gov Identifier: NCT00470756  
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

ClinicalTrials.gov processed this record on February 12, 2009