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Foot Deformities clinical trials

View clinical trials related to Foot Deformities.

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NCT ID: NCT02093507 Recruiting - Clinical trials for Foot Deformity Congenital

Effectiveness of Parent's Manipulation in Newborn With Metatarsus Adducts. a Randomized Controlled Trial

Start date: May 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the result of parent's feet manipulation compared with nonmanipulated group within first 6 months of life and observe spectrum of the disease within this period.

NCT ID: NCT00624299 Withdrawn - Foot Deformities Clinical Trials

Botox Clinical Trial

Start date: March 2008
Phase: Phase 4
Study type: Interventional

The surgery to correct leg & foot deformities in children is a lengthy, & sometimes, difficult procedure. Metal frames are attached to the leg and / or foot and over a period of time the frame is manipulated to obtain the corrected position. During this period the muscles & skin become very tight which causes pain & may pull the joint out of position. When this happens it is sometimes necessary to stop the treatment before the best position is obtained. This means that not only is the child left with an inadequate result but that further surgery is required in the future. If the tension could be removed whilst the treatment is underway this would reduce the pain, the possibility of joint damage & potentially allow a more satisfactory to be obtained without the need for further surgery. Botulinum toxin or Botox, as it is commonly called, has the potential to temporarily reduce the tension in the muscles without causing permanent damage.

NCT ID: NCT00499356 Completed - Diabetes Clinical Trials

Shear and Pressure Reducing Insoles for the Diabetic Foot

GlideSoft
Start date: May 2002
Phase: N/A
Study type: Interventional

We evaluated the feasibility of the GlideSoft™ novel insole to reduce pressure and shear forces on the foot. No commercially available insoles are designed to reduce shear. Although insurance providers spend millions on diabetics’ therapeutic insoles, there is no scientific data about shear or pressure reduction. We will evaluate the optimal bonded materials from Phase I compared to the Glidesoft™ design using the same combination of viscoelastic materials. We evaluate 2 patient groups of 150 patients per arm (300 total) in an 18 month trial. The control group patient arm wore a traditional bonded insole whereas another the second arm receive the GlideSoft™. At baseline, and at the end of the 18 month trial, in-shoe gait lab and in vitro biomechanical parameters measured pressure, shear, and material properties as these changed with wear. This Phase II eighteen (18) month clinical trial evaluated the effectiveness of ShearSole™ reducing the incidence of diabetic ulcers. The overall study hypothesis was that GlideSoft™ provides significant shear reduction as compared to traditional insoles without sacrificing pressure reduction characteristics or durability.

NCT ID: NCT00475631 Withdrawn - Clubfoot Clinical Trials

Economic Evaluation of Clubfoot Treatment: One Centre's Experience

Start date: October 2003
Phase:
Study type: Observational

Purpose: The purpose of the study is to complete a cost analysis of the different methods used for clubfoot treatment. Objectives: Short-term objective: To explore the experience of British Columbia Children's Hospital (BCCH) with costs and outcomes related to the various forms of clubfoot management since 1984 to present. Long-term objective: To use the information gathered in this project and apply it to future studies in the clubfoot research program and to do a complete cost-benefit analysis. Hypothesis: The hypothesis of the study is that the BCCH clubfoot treatment program has better outcomes in terms of reduced financial costs than the traditional surgical management.

NCT ID: NCT00474344 Completed - Clubfoot Clinical Trials

Genetic Linkage Study of Idiopathic Talipes Equinovarus (ITEV) (Clubfoot)

Start date: August 2004
Phase:
Study type: Observational

The goal of this study is to identify and characterize the genetic loci causing idiopathic talipes equinovarus (clubfoot). The hypothesis is that a few genes account for a substantial fraction of ITEV and that these genes can be identified in defined populations. Towards this goal, in preliminary studies, Dr. Hecht's group has identified two genes, NAT2 and CASP10, which demonstrate evidence for linkage and association to ITEV.

NCT ID: NCT00474032 Recruiting - Clubfoot Clinical Trials

Using Botox to Treat Patients With Idiopathic Clubfoot

Start date: March 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effectiveness of treatment of idiopathic clubfoot utilizing Botulinum Toxin Type A (Botox). This is not a hypothesis-generating study as we are reporting on outcomes of patients who have been treated by this method of clubfoot treatment.

NCT ID: NCT00175708 Completed - Clubfoot Clinical Trials

Pedobarographic Assessments of Clubfoot Treated Patients

Start date: September 2005
Phase:
Study type: Observational

The purpose of this study is to determine the utility of pedobarographs in evaluating clubfoot post-treatment.