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Muscular Atrophy clinical trials

View clinical trials related to Muscular Atrophy.

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NCT ID: NCT01717651 Terminated - Respiratory Failure Clinical Trials

Muscle Atrophy in Patients With Severe Sepsis

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

This study is being done to help determine whether patients with severe sepsis (overwhelming inflammation in the body as a result of an infection) lose muscle and become weak more rapidly than patients with other severe illnesses. Weakness and muscle loss that develops after a severe illness is a serious problem. Patients who develop weakness and have a decrease in muscle size often have to stay in the hospital longer and have a higher chance of dying. At the current time, it is not clear whether certain severe illnesses are more likely to cause weakness and muscle loss. This study will be done to measure the changes in muscle size and strength as a result of each patient's illness

NCT ID: NCT01547871 Terminated - Clinical trials for Spinal Muscular Atrophy

Infants With Spinal Muscular Atrophy Type I

Start date: February 7, 2012
Phase:
Study type: Observational

Background: - Spinal muscular atrophy type 1 (SMA 1) causes severe muscle weakness and problems with eating and breathing. The symptoms begin in infancy, and children affected with SMA 1 often die in early childhood. Researchers want to collect information on how SMA symptoms progress in first two years. Objectives: - To study how the symptoms of SMA 1 progress in infants and children. Eligibility: - Infants and children with SMA 1 born on or after January 1, 2007. Design: - Researchers will review the child s medical records and talk with parents by telephone. - For children who are under 2 years of age, the researchers will review the child s medical records and speak with you on telephone every 2-4 months. Phone calls with parents will take about 10 minutes and will involve questions about symptoms of SMA 1. Children will be followed until age 2.- Researchers are also interested in looking at medical records of children who are no longer alive or who are more than 2 years of age. Parents or children do not have to come to the NIH. They will provide consent to view these records, and information over the telephone. - No treatment or care will be provided as part of this study.

NCT ID: NCT01524406 Terminated - Muscle Atrophy Clinical Trials

Safety Study of HPP593 in Subjects During and After Limb Immobilization

Start date: January 2012
Phase: Phase 1
Study type: Interventional

This is a safety and tolerability study investigating the effect of HPP593 in healthy volunteers during and after limb immobilization.

NCT ID: NCT01388920 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Efficacy and Safety Study of Tesamorelin in Chronic Obstructive Pulmonary Disease (COPD) Subjects With Muscle Wasting

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

A significant proportion of COPD subjects experience muscle wasting, which has been associated with increased morbidity, impaired physical functioning, and a poor quality of life. Muscle wasting is associated with reduced muscle strength in COPD subjects. In particular, weakness of peripheral muscles has been reported to play an important role in the reduced functional capacity and impaired exercise performance. The primary objective of this study is to investigate the effect of tesamorelin, in conjunction with exercise training, on lean body mass measured by dual energy x-ray absorptiometry (DXA) scan.

NCT ID: NCT00439569 Terminated - Clinical trials for Spinal Muscular Atrophy Type II

Clinical Trial of Sodium Phenylbutyrate in Children With Spinal Muscular Atrophy Types II or III

NPTUNE01
Start date: January 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to identify the maximum tolerated dosage of sodium phenylbutyrate in children with spinal muscular atrophy types II or III; and to determine if the drug has an effect on SMN mRNA and protein levels.

NCT ID: NCT00439218 Terminated - Clinical trials for Spinal Muscular Atrophy Type I

Clinical Trial of Sodium Phenylbutyrate in Children With Spinal Muscular Atrophy Type I

NPTUNE 02
Start date: January 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to identify the maximum tolerated dosage of sodium phenylbutyrate in children with spinal muscular atrophy type I; and to determine if the drug has an effect on SMN mRNA and protein levels.