Actively Recruiting

Phase Not Applicable
Age: 1Day - 12Months
All Genders
NCT07428902

Effects Of French Method With/Without Brace In Clubfoot Treatment

Led by Riphah International University · Updated on 2026-02-24

18

Participants Needed

1

Research Sites

16 weeks

Total Duration

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AI-Summary

What this Trial Is About

The current study will be a randomized control trial. Data will be collected from the Pakistan Society for the Rehabilitation of the Disabled, Lahore (PSRD) and the Children Hospital and Institute of Child Health, Lahore. The study will include 18 patients, equally divided into two groups and randomly allocated. Inclusion criteria will be children aged 0 to 12 months diagnosed with CTEV of either gender. Patients with neurological conditions, other orthopedic issues, previous surgical history related to the foot, severe systemic disorders, or neuromuscular disorders will be excluded from the study. The experimental group will receive the French method along with a foot abduction brace, while the control group will receive only the French method without the brace. Outcomes to be analyzed will include foot position, severity of deformity, and functional mobility. Data collection will occur before and after the intervention, utilizing clinical assessments for foot position, the Pirani score for severity of deformity, and standardized mobility assessments. Data will be analyzed using SPSS version 23.00.

CONDITIONS

Official Title

Effects Of French Method With/Without Brace In Clubfoot Treatment

Who Can Participate

Age: 1Day - 12Months
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients under 12 months of age with clubfeet.
  • All patients without previous clubfoot surgery were included.
  • Children who have not received any prior corrective treatment or bracing for CTEV.
Not Eligible

You will not qualify if you...

  • Patients with prior clubfoot surgery were excluded.
  • Non-idiopathic cases with underlying conditions were excluded due to poor response to nonoperative treatment.

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Trial Site Locations

Total: 1 location

1

Pakistan Society for the Rehabilitation of the Disabled

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

I

IMRAN AMJAD, PhD

CONTACT

M

Muhammad Asif Javed, MS-PT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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