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6 studies found for:    "Arthrogryposis multiplex congenita"
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"Arthrogryposis multiplex congenita" (6 records)
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Rank Status Study
1 Unknown  Study of Resting and Exercising Body Functioning in Freeman-Sheldon Syndrome and Related Conditions
Conditions: Arthrogryposis;   Craniofacial Abnormalities
Interventions: Other: Lactate, Glucose, and Adenosine Triphosphate Blood Levels;   Procedure: Physiological Stress Test;   Other: Functional Enquiry Form;   Other: Strength, Joint ROM, Girth and Length Measurements;   Other: Study Physical Examination;   Other: Observational Gait Analysis;   Other: Mental Health Interview
2 Unknown  Survey Study and Records Review of Treatment Outcomes in Freeman-Sheldon Syndrome
Conditions: Arthrogryposis;   Craniofacial Abnormalities
Interventions: Other: STOP-FSS Survey;   Other: Medical Records Review
3 Enrolling by invitation WREX Outcome Study
Conditions: Muscular Dystrophy;   Arthrogryposis;   Spinal Muscular Atrophy
Intervention: Device: WREX orthosis
4 Completed Effects of Power Mobility on Young Children With Severe Motor Impairments
Conditions: Cerebral Palsy;   Arthrogryposis;   Spinal Muscular Atrophy;   Other Central Nervous System or Musculoskeletal Disorders
Intervention: Other: Power mobility
5 Unknown  Study of Quality of Life in Freeman-Sheldon Syndrome and Related Conditions
Conditions: Arthrogryposis;   Craniofacial Abnormalities;   Posttraumatic Stress Disorder;   Depressive Disorder
Interventions: Other: PTSD Checklist-Specific;   Other: Modified Flanagan Quality of Life Scale;   Other: Center for Epidemiologic Studies Depression Scale;   Other: Functional Enquiry Form;   Other: Strength, Joint ROM, Girth and Length Measurements;   Other: Study Physical Examination;   Other: PTSD, Depression, and FSS-Focused Examination;   Other: Freeman-Sheldon Specific Quality of Life Survey;   Other: Lactate, Glucose, and Adenosine Triphosphate Blood Levels
6 Completed Movement Enhancing Device for Children
Condition: Upper Extremity Dysfunction
Intervention: Device: Movement Enhancing Device

Study has passed its completion date and status has not been verified in more than two years.