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Clubfoot clinical trials

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NCT ID: NCT02257229 Recruiting - Clubfoot Deformity Clinical Trials

Prospective Evaluation of Treatment for Clubfoot

Start date: August 2005
Phase:
Study type: Observational

Specific aim: To evaluate the outcome of infants who undergo one of two nonsurgical treatment interventions

NCT ID: NCT02233140 Recruiting - Diabetes Clinical Trials

Effectiveness of Manual Manipulation With EPAT on Ankle Dorsiflexion and Dynamic Plantar Pressure

Start date: October 2014
Phase: N/A
Study type: Interventional

Diabetic foot complications are a common and costly problem. Excessive plantar pressures due to foot deformities and/or limited ankle dorsiflexion, especially in the presence of peripheral neuropathy, can predispose subjects with diabetes for diabetic foot ulcers. Achilles tendon lengthening surgery has shown to delay or prevent recurrence of diabetic foot ulcers. Studies have shown that Shockwave Therapy (EPAT - Extracorporeal Pulse Activation Technology) was effective in treating subjects with chronic heel pain and Achilles tendonitis with no serious side effects. EPAT, therefore, may allow diabetic patients with ankle equinus to perform more effective stretching exercises and may prevent recurrence of diabetic foot ulcers. The purposed of this RCT is to compare effectiveness of manual manipulation with EPAT versus manual manipulation alone on ankle dorsiflexion and dynamic plantar pressure in at-risk subjects with a history of diabetic foot ulcer.

NCT ID: NCT02188277 Completed - Cerebral Palsy Clinical Trials

Treatment With Xeomin Versus Botox in Children With Spastic Equine and Equinovarus Foot Deformation in Pediatric Cerebral Palsy

XEBEC
Start date: July 2014
Phase: Phase 2
Study type: Interventional

1. To assess the clinical and neurophysiological efficacy of Xeomin® vs. Botox® in children with spastic equine and equinovarus foot deformation in pediatric cerebral palsy 2. To assess the safety of Xeomin® use as compared to Botox® in this patient population

NCT ID: NCT02051933 Terminated - Equinus Contracture Clinical Trials

The Effect of Botulinum Toxin A Injections on Ankle Dorsiflexion Following Internal Fixation of Tibial Pilon Fractures

Botox
Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if botulinum toxin type A (Botox) injections, at the time of surgery for pilon fractures, will improve ankle range-of-motion and functionality.

NCT ID: NCT02022267 Completed - Clubfoot Clinical Trials

Gait Analysis in Ponseti Clubfoot

Start date: October 2011
Phase: N/A
Study type: Observational

Patients with clubfoot treated with the Ponseti method from a prospective database are evaluated using gait analysis including a foot model and a disease specific instrument score and compared to a group of healthy children.

NCT ID: NCT01767662 Recruiting - Clinical trials for Talipes Calcaneovalgus

Effectiveness of Parents' Manipulation in Newborn With Talipes Calcaneus

Start date: May 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine effectiveness of parents' manipulation in newborn with talipes calcaneovalgus over observation group.

NCT ID: NCT01551264 Completed - Isolated Clubfoot Clinical Trials

Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial

FAB24
Start date: May 2012
Phase: N/A
Study type: Interventional

The goal of this multi-center, randomized, controlled trial is to evaluate the effectiveness of a 2 year versus 4 year bracing protocol in preventing isolated clubfoot recurrence within the first year post-treatment, and to evaluate factors associated with recurrence in isolated clubfoot.

NCT ID: NCT01481324 Completed - Clubfoot Clinical Trials

Outcomes of Compliance With Brace Wear in Clubfoot

Start date: October 2009
Phase: N/A
Study type: Observational

It has been shown that compliance with brace wear can significantly improve the treatment outcome of idiopathic clubfoot deformities. Noncompliance rates have been estimated to be around 30-41% with initial orthosis wear after successful treatment with serial castings. These studies have depended on family logs and not objective data. With the development of a monitoring device, this study hopes to examine: (1) actual patient compliance, (2) comparisons of actual wear time and assumed wear time and (3) the relationship of patient wear with clinical outcomes. Hypothesis: Actual patient compliance in foot abduction orthoses (FAO) wear is less than self-reported compliance and noncompliance is correlated to future surgeries.

NCT ID: NCT01382628 Completed - Clinical trials for Diabetic Foot Ulcers

Determination of the Pathophysicologic Collagen Changes in the Diabetic Achilles Tendon

Start date: May 2011
Phase:
Study type: Observational

This is a pilot study examining tendon collagen, collagen cross-linking, and markers of tendon extracellular matrix metabolism in the Achilles tendon of diabetic patients with ulcerations and amputations of the lower extremity.

NCT ID: NCT01265238 Completed - Stroke Clinical Trials

Neuro-orthopaedic Surgery in the Treatment of the Spastic Equinovarus Foot

Start date: December 2009
Phase: N/A
Study type: Observational

Spastic equinovarus foot (SEF) is a major cause of disability in stroke patients. Treatments may include physical therapy, orthosis, botulinum toxin (BTX) injections, selective tibial neurotomy and tendon lengthening and/or transfer. Until now, no study has been conducted to assess the result of neuro-orthopaedic surgery in the treatment of SEF. The aim of this study is to evaluate the benefit of neuro-orthopaedic surgery (selective neurotomy and/or Achilles tendon lengthening and/or tibialis anterior transfer) in case of SEF according to the 3 domains of the International Classification of Functioning, Disability and Health (ICF)of the World Health organisation (WHO)