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

Clubfoot Clinical Trial

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03749265
• Other study ID #: EMC-0010-18
• Status: Not yet recruiting
• Start date: December 2018
• Est. completion date: October 2019

Study information

• Verified date: December 2018
• Source: HaEmek Medical Center, Israel
• Contact: Eytan Dujovni, senior
• Phone: +97254761-1961
• Email: eytan_du[@]clalit.org.il
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 75
• Est. completion date: October 2019
• Est. primary completion date: August 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 5 Years to 120 Years

Eligibility

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

Related Conditions & MeSH terms

• Clubfoot
• Equinus Deformity

Intervention

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

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
HaEmek Medical Center, Israel

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Presence or Absence of peroneus tertius		1 hour