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Rate Of Residual Clubfoot Deformity With Correlation To Absence Of Peroneus Tertius Muscle

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03749265
Recruitment Status : Not yet recruiting
First Posted : November 21, 2018
Last Update Posted : December 5, 2018
Sponsor:
Information provided by (Responsible Party):
Eytan Dujovny, HaEmek Medical Center, Israel

Brief Summary:
Rate Of Residual Clubfoot Deformity With Correlation To Absence Of Peroneus Tertius Muscle , A Prospective Study.

Condition or disease Intervention/treatment
Clubfoot Other: Ultrasound test

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Study Type : Observational
Estimated Enrollment : 75 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Rate Of Residual Clubfoot Deformity With Correlation To Absence Of Peroneus Tertius Muscle: A Prospective Study
Estimated Study Start Date : December 2018
Estimated Primary Completion Date : August 2019
Estimated Study Completion Date : October 2019

Intervention Details:
  • Other: Ultrasound test
    patients need to undergo an ultrasound test for detecting the presence or abscence of peroneus tertius tendon


Primary Outcome Measures :
  1. Presence or Absence of peroneus tertius [ Time Frame: 1 hour ]


Information from the National Library of Medicine

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Ages Eligible for Study:   5 Years to 120 Years   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Patients aged 5-17 years , which were treated with the Ponseti technique for Clubfoot in HaEmek medical center, and have sufficient data/follow-up about them in medical records
Criteria

Inclusion Criteria:

  • patients aged 5-17 years , which were treated with the Ponseti technique for Clubfoot in HaEmek medical center, and have sufficient data/follow-up about them in medical records /

Exclusion Criteria:

  • patients aged< 5 years
  • Neurological Clubfoot
  • patients with insufficient data in medical records
  • clubfoot caused by arthrogryposis , connective tissue diseases and congenital fibular hemimelia

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03749265


Contacts
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Contact: Eytan Dujovni, senior +97254761-1961 eytan_du@clalit.org.il

Sponsors and Collaborators
HaEmek Medical Center, Israel
Investigators
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Principal Investigator: Eytan Dujovni, senior haemek medical center
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Responsible Party: Eytan Dujovny, Senior doctor in orthopedics department, HaEmek Medical Center, Israel
ClinicalTrials.gov Identifier: NCT03749265    
Other Study ID Numbers: EMC-0010-18
First Posted: November 21, 2018    Key Record Dates
Last Update Posted: December 5, 2018
Last Verified: December 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Eytan Dujovny, HaEmek Medical Center, Israel:
Peroneus Tertius Muscle
Additional relevant MeSH terms:
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Clubfoot
Talipes
Equinus Deformity
Congenital Abnormalities
Foot Deformities, Acquired
Foot Deformities
Musculoskeletal Diseases
Foot Deformities, Congenital
Lower Extremity Deformities, Congenital
Limb Deformities, Congenital
Musculoskeletal Abnormalities