Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05767762
Other study ID # 22-HPNCL-09
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 26, 2023
Est. completion date December 2031

Study information

Verified date March 2023
Source Fondation Lenval
Contact Grégoire Peuchevrier
Phone 492030323
Email peuchevrier.g@hpu.lenval.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Clubfoot is an orthopedic congenital malformation of the lower limb of the newborn evaluated by the Dimeglio score. There is a deficit of muscular balance between the agonists and antagonists to the deformity. The Dimeglio score takes into account the muscular activity but only up to one point out of 20. This study proposes to use a muscle scale inspired by the Dimeglio score to see if there is a correlation between muscle activity and the risk of tenotomy before 1 year. It will also assess the inter-examiner reproducibility of this scale. This study is a prospective cohort study with a duration of 8 years to include about 100 feet. Infants with idiopathic Clubfoot treated with the functional method at up to 15 days of life will be included. Feet will be assessed at an inclusion visit and then at 3-6-12 months. The primary endpoint will be the need for Achilles tenotomy before 1 year of age. The secondary endpoint will be inter-examiner reproducibility determined by statistical analysis. The expectation of this study would be to define a predictive factor of the evolution of the PBVE in order to refine the treatment earlier.


Description:

Clubfoot is a congenital orthopedic deformity of the lower limb in newborns. It is characterized by a triple deformity of the foot: equinus, supination and adduction of the forefoot. It can be bilateral or unilateral. PBVE can be idiopathic or associated with another etiology such as neurological, rheumatological, etc. There is a muscular hypoplasia of the muscles antagonistic to the PBVE and an imbalance of force between the agonists and antagonists to the benefit of the deformity. There is also an abnormality of the fibular and posterior tibial nerves. The aim of the study is the muscular evaluation of the PBVE. The scientific literature is relatively poor on the subject. In the first year of life, if the articular evaluation of the PBVE is very precise, the muscular scoring seems less well taken into account. In the Dimeglio score, the muscular criterion counts for 1 point (against 16 articular points) if it is possible to obtain a muscular contraction of the antagonists. It does not specify which muscles are present nor the active reducibility of the deformity. A scale based on the Dimeglio score has been created to evaluate muscle activity. To fill it out, the practitioner will have to stimulate the muscles antagonistic to the deformity by tactile stimulation. This will be an 8-year prospective cohort study that will look for a correlation between the muscle deficit and the risk of tenotomy before 1 year as well as the quality of inter-examiner reproduction of the scale. This duration is necessary to obtain a sufficient number of inclusions (100 feet). Infants with idiopathic Clubfoot treated with the functional method at up to 15 days of life will be included. At the first consultation, we will perform the Dimeglio score and our muscle activity scale. The Dimeglio and the muscle activity scale will be performed at 3, 6 and 12 months. The population included will need to be sufficient to ensure that all levels of muscle scoring are represented. The primary endpoint will be the need for Achilles tenotomy before 1 year. The secondary endpoint will be inter-examiner reproducibility determined by statistical analysis. The expectation of this study would be to define a predictive factor of the evolution of the PBVE in order to refine the treatment earlier.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 2031
Est. primary completion date March 2031
Accepts healthy volunteers No
Gender All
Age group 0 Months to 12 Months
Eligibility Inclusion Criteria: - idiopathic clubfoot, managed by the functional method, managed before D15 to perform the initial assessment. Exclusion Criteria: - syndromic clubfoot, management other than functional method, management after D15

Study Design


Related Conditions & MeSH terms


Intervention

Other:
scale Idiopathic Clubfoot
The Dimeglo and the muscle activity scale will be performed at 3, 6 and 12 months with patient with idiopathic clubfoot

Locations

Country Name City State
France Hopitaux Pediatriques de Nice Chu-Lenval Nice

Sponsors (1)

Lead Sponsor Collaborator
Fondation Lenval

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Surgery number of patient who need for Achilles tenotomy maximum 1 year after inclusion
Secondary Inter-examiner reproducibility measure with statistical study the Inter-examiner reproducibility through study completion, an average of 8 years
See also
  Status Clinical Trial Phase
Withdrawn NCT03580746 - Comparison of Ponseti Method Versus Older Treatments in Talipes Equinovarus Through Gait Analysis and Clinical Results
Completed NCT00175708 - Pedobarographic Assessments of Clubfoot Treated Patients
Recruiting NCT06050746 - Predictive Value of the PBS-score in Children With Clubfoot
Recruiting NCT06050564 - Therapeutic Recommendations Based on Clinical History and Video Documented PBS-Score
Recruiting NCT06033638 - Video Documented PBS-Score in Children With Clubfoot
Completed NCT02022267 - Gait Analysis in Ponseti Clubfoot N/A
Completed NCT01481324 - Outcomes of Compliance With Brace Wear in Clubfoot N/A
Withdrawn NCT00475631 - Economic Evaluation of Clubfoot Treatment: One Centre's Experience
Completed NCT01088828 - Exploring the Causes of Clubfoot Using Magnetic Resonance Imaging, MRI N/A
Completed NCT02815306 - Polyaxial Brace Fixing for the Treatment of Congenital Clubfoot N/A
Not yet recruiting NCT01050088 - Sucrose Analgesia in Infants Undergoing Casting for Club Foot N/A
Recruiting NCT00474032 - Using Botox to Treat Patients With Idiopathic Clubfoot N/A
Recruiting NCT04564430 - Clonidine for Tourniquet-related Pain in Children Phase 4
Recruiting NCT03249805 - MiracleFeet Foot Abduction Brace Sensor Trial N/A
Recruiting NCT04766684 - Comparison Study of LMX4 Cream Versus J-Tip Needle-Free Injection System With Lidocaine for In-Office PAT for Clubfoot Phase 4
Not yet recruiting NCT04737083 - CGH Array in Bilateral Clubfoot
Completed NCT02395185 - A Randomized Controlled Trial of Three Non-pharmacologic Analgesic Techniques for Casting of Clubfoot Infants N/A
Completed NCT00607191 - Clubfoot DNA Repository N/A
Completed NCT05456737 - Functional Assessment in Children With Clubfoot
Active, not recruiting NCT04693065 - Pronostic Factors of Long Term Outcome in Patients With Clubfoot Treated by the Ponseti Method