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Status unknownNCT03749265Updated Dec 5, 2018

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

An observational study in Clubfoot, sponsored by HaEmek Medical Center, Israel. Status unknown. Open to participants aged 5 Years to 120 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-12-05.

Sponsored by HaEmek Medical Center, Israel · Observational

The sponsor has not verified this record recently (last verified Dec 2018), so the status shown — last known as Not yet recruiting — may be out of date.

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Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
75
Ages
5 Years to 120 Years
Sex
All
01

Study summary

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

02

Conditions studied

  • Clubfoot

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Keywords

  • Peroneus Tertius Muscle
03

In context

Clubfoot

69 studies on the registry are indexed under Clubfoot; 15 are open to participants now.

This study's planned enrollment of 75 is above the median of 55 across 27 observational studies indexed under Clubfoot.

Browse Clubfoot studies →

Lead sponsor

HaEmek Medical Center, Israel is the lead sponsor of 237 studies on the registry; 11 are open to participants now.

Browse HaEmek Medical Center, Israel studies →

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years to 120 Years
Sexes eligible
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

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
75 participants (estimated)
Patient registry
No

Interventions

  • OtherUltrasound test

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

06

What researchers measure

Primary outcomes

  1. Presence or Absence of peroneus tertius

    Time frame: 1 hour

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Dec 2018; primary completion for Aug 2019, 8 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 20, 2018
First posted
Nov 21, 2018
StartEst.
Dec 2018
Primary completionEst.
Aug 2019
CompletionEst.
Oct 2019
Last update
Dec 5, 2018
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Dec 5, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03749265
Lead sponsor
HaEmek Medical Center, Israel
Responsible party
Eytan Dujovny (Senior doctor in orthopedics department, HaEmek Medical Center, Israel) — Principal investigator
First posted
Nov 21, 2018
Start date
Dec 2018 (estimated)
Primary completion
Aug 2019 (estimated)
Completion
Oct 2019 (estimated)
Last update
Dec 5, 2018

Study contacts

Eytan Dujovni, senior
Contact
eytan_du@clalit.org.il
+97254761-1961
Eytan Dujovni, senior
principal investigator · haemek medical center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2018. You cannot join it, but the record below documents what was studied.

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Discussion

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