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Contracture clinical trials

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NCT ID: NCT01512082 Completed - Clinical trials for Contracture of Muscle, Thigh

The Effect of Reducing Soreness in Marathon Runners

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

Delayed onset muscle soreness is defined as the sensition of pain and discomfort in skeletal muscles that occurs after eccentric muscle actions or strenuous exercise like a marathon.

NCT ID: NCT01498640 Completed - Dupuytren's Disease Clinical Trials

Retreatment of Recurrent Dupuytren's Contractures

Start date: March 2012
Phase: Phase 4
Study type: Interventional

The objectives of this study are to assess the safety and efficacy of AA4500 in the retreatment of recurrent contractures in joints that were effectively treated with AA4500 in a previous Auxilium-sponsored Phase 3 study.

NCT ID: NCT01450397 Completed - Dupuytren's Disease Clinical Trials

MRI Results in Dupuytren's Contracture Before and After Injection With Xiaflex

Start date: March 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effects of XIAFLEX on your finger through MRI.

NCT ID: NCT01444729 Completed - Clinical trials for Dupuytren's Contracture

Post Approval Commitment Study

Start date: March 2012
Phase: N/A
Study type: Observational

An agreement has been made to conduct a post-approval commitment study that provides supplementary information relating to the use of Xiapex® as well as other non-pharmacological treatments for Dupuytren's contracture by health care professionals in a real world clinical setting.

NCT ID: NCT01407068 Completed - Clinical trials for Dupuytren's Contracture

Administration of Two Injections for Multiple Dupuytren's Contractures

Start date: September 2011
Phase: Phase 3
Study type: Interventional

The objectives of this study are to assess the safety and efficacy of concurrent administration of two injections of AA4500 into the same hand of subjects with multiple Dupuytren's contractures caused by palpable cords.

NCT ID: NCT01403402 Recruiting - Clinical trials for Limb-Girdle Muscular Dystrophy

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

CMDPROS
Start date: September 2009
Phase:
Study type: Observational [Patient Registry]

The Congenital Muscle Disease Patient and Proxy Reported Outcome Study (CMDPROS) is a longitudinal 10 year study to identify and trend care parameters, adverse events in the congenital muscle diseases using the Congenital Muscle Disease International Registry (CMDIR) to acquire necessary data for adverse event calculations (intake survey and medical records curation). To support this study and become a participant, we ask that you register in the CMDIR. You can do this by visiting www.cmdir.org. There is no travel required. The registry includes affected individuals with congenital muscular dystrophy, congenital myopathy, and congenital myasthenic syndrome and registers through the late onset spectrum for these disease groups. The CMDIR was created to identify the global congenital muscle disease population for the purpose of raising awareness, standards of care, clinical trials and in the future a treatment or cure. Simply put, we will not be successful in finding a treatment or cure unless we know who the affected individuals are, what the diagnosis is and how the disease is affecting the individual. Registering in the CMDIR means that you will enter demographic information and complete an intake survey. We would then ask that you provide records regarding the diagnosis and treatment of CMD, including genetic testing, muscle biopsy, pulmonary function testing, sleep studies, clinic visit notes, and hospital discharge summaries. Study hypothesis: 1. To use patient and proxy reported survey answers and medical reports to build a longitudinal care and outcomes database across the congenital muscle diseases. 2. To generate congenital muscle disease subtype specific adverse event rates and correlate with key care parameters.

NCT ID: NCT01320124 Withdrawn - Osteoarthritis Clinical Trials

Creating a Tissue Bank of Knee Capsules

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

A contracture is a pathological condition limiting range and function of joints. Contractures of large and small joints alike will affect one's ability to independently perform daily activities such as eating, dressing or walking. Current treatments for contractures include physical stretching, the use of assistive devices or, rarely, surgery. Despite prolonged treatments, patients with contractures rarely regain complete mobility. Progress in preventing and treating contractures will be possible only through an understanding of the biological and molecular processes involved. Our group has established and validated an animal model to study the histological events and the molecular mechanisms involved in joint contractures. We have provided evidence for capsule stiffness, characterized cartilage degeneration, and identified four genes whose expression is altered in the cartilage of a knee joint with contracture. The work we propose in the current study aims at finding genes and pathways in the joint capsule associated with knee joint contractures. The results will identify new avenues for treating the large number of patients suffering from contractures.

NCT ID: NCT01265420 Completed - Clinical trials for Dupuytren's Contracture

Efficacy and Safety of Xiaflex Injection for Treatment of Dupuytren's Contracture of the Thumb

Start date: December 2010
Phase: Phase 4
Study type: Interventional

This study will evaluate the efficacy and safety of clostridial collagenase injections for treatment of Dupuytren's contracture of the thumb and first web space. The investigators hypothesis is that clostridial collagenase will have safety not significantly different to that demonstrated in Phase III clinical trials, and will be effective in significantly reducing the degree of thumb contracture.

NCT ID: NCT01238484 Terminated - Diabetes Mellitus Clinical Trials

Ankle Equinus Contracture Treated With Dynamic Splinting

Start date: August 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the Ankle Dorsiflexion Dynasplint System (DS) is effective in treating contracture for patients with Ankle Equinus secondary to diabetes mellitus.

NCT ID: NCT01237964 Not yet recruiting - Clinical trials for Burn's Associated Contracture

Injectable Collagenase For Burns' Associated Contracture

Start date: March 2011
Phase: Phase 2
Study type: Interventional

A pilot experiment to test the efficiency of the enzyme Collagenase in treating contractures which result's from burn's healing process. So far, treatment of choice in patients with burn's created movement limiting contractures, concentrated around supportive care. Patients were referred to surgical intervention only if necessary. Treatment by injecting an external enzyme is avant-garde and hasn't been done under such conditions. This study might introduce a new kind of treatment, which can be done in ambulatory environment .This type of treatment might significantly improve patients' function and quality of life, with no need for a surgical intervention.