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Muscular Atrophy clinical trials

View clinical trials related to Muscular Atrophy.

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NCT ID: NCT02227823 Completed - Clinical trials for Spinal Muscular Atrophy Type 3

Safety and Efficacy Study of Pyridostigmine on Patients With Spinal Muscular Atrophy Type 3

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

The purpose of this study is to evaluate safety and efficacy of anti-cholinesterase therapy on the motor function in SMA type 3 patients with impaired neuromuscular junction (NMJ).

NCT ID: NCT02218593 Completed - Clinical trials for Spinal Muscular Atrophy

WREX Outcome Study

Start date: July 2014
Phase:
Study type: Observational

This study is to evaluate how the Wilmington Robotic Exoskeleton (WREX) is working for children who are using the WREX, or have used it in the past. The survey consists of a set of questions a) performed online and b) performed over the phone.

NCT ID: NCT02174029 Completed - Clinical trials for Muscle Atrophy or Weakness

Serial Daily Diaphragm Ultrasounds in Ventilated Patients

Start date: June 2014
Phase: N/A
Study type: Observational

When a person is put on a breathing machine the investigators think that the breathing muscles can get weaker. The investigators are not sure how quickly this happens but in some people this leads to problems when they try to breathe on their own without the breathing machine. The diaphragm is at the bottom of a person's chest separating their lungs from what is in their belly and it is a very strong muscle. In fact, it is main muscle that one uses for breathing. An ultrasound machine is a painless way to see what is happening beneath the skin. It is safe and easy to do. Using an ultrasound the investigators are planning to measure how thick the diaphragm is and how much it changes while a person is on a breathing machine in the ICU. Getting a better understanding of this condition could lead to improved treatments that might help support patients who require a ventilator for breathing. The investigators hypothesis is that patients for whom the breathing machine is doing all of the work of breathing, will have their diaphragm thickness gradually decrease and changing to a breathing modem mode where they have to put in more effort the diaphragm thickness will start increasing again.

NCT ID: NCT02156141 Completed - Healthy Subjects Clinical Trials

High Intensity Training in Patients With Spinal and Bulbar Muscular Atrophy

HIT in Kennedy
Start date: June 2014
Phase: N/A
Study type: Interventional

We want investigate if high intensity training can increase daily functionality without causing muscle damage in patients Spinal and Bulbar Muscular Atrophy . We want to study if there is a difference in effect with supervised and unsupervised training. Furthermore we want to study if a supervised training program will motivate participants to continue training by the end of the program.

NCT ID: NCT02152761 Completed - Clinical trials for Muscle Wasting (Atrophy) After Hip Fracture Surgery

Study of Efficacy and Safety of Bimagrumab in Patients After Hip Fracture Surgery

Start date: September 16, 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study was to assess if bimagrumab is safe and effective in patients with muscle wasting (atrophy) after hip fracture surgery.

NCT ID: NCT02124057 Completed - Clinical trials for Motor Neuron Disease

Study of Hepatic Function in Patients With Spinal and Bulbar Muscular Atrophy

Start date: August 4, 2014
Phase:
Study type: Observational

Background: - Spinal and bulbar muscular atrophy (SBMA) is an inherited disease. It causes weakness in muscles used for swallowing, breathing, and speaking. SBMA mainly affects men, but women can carry the gene for it. Researchers think there may be a link between SBMA and excess fat in the liver. Objective: - To look for fatty liver and liver injury in people with SBMA, people with motor neuron disease, and people who carry the gene for SBMA. Eligibility: - Adults 18 years and older who have SBMA, have motor neuron disease, or are carriers of SBMA. - Healthy adult volunteers. Design: - Participants will be screened with medical history, physical exam, and blood tests. - Participants will have 1 outpatient visit of 1-2 days. Women will have a urine pregnancy test. All participants will have: - Blood tests. - Liver ultrasound. A probe is placed on the abdomen at certain locations and angles and takes pictures. The painless procedure takes 20-30 minutes. - Liver magnetic resonance imaging (MRI) scan. The MRI scanner is a metal cylinder with a magnetic field. Participants will lie on a table that slides in and out of it. They will be in the scanner for about 30 minutes. They will get earplugs for loud noises. - Some participants with abnormal liver testing will have a biopsy (small piece) of the liver taken. The biopsy site will be located with ultrasound, then cleaned and numbed. The physician will quickly pass a needle in and out of the liver while the participants holds their breath. Afterward, participants will be monitored in bed for 6 hours. - Participants may return for follow-up and another 1-2 day outpatient visit yearly for up to 2 years.

NCT ID: NCT02123186 Completed - Clinical trials for Spinal Muscular Atrophy

Newborn Screening for Spinal Muscular Atrophy

Start date: October 2013
Phase: N/A
Study type: Observational

To test if the routine newborn screening dried blood spots can be used to test if missing 2 copies of SMN1 gene, a status indicating spinal muscular atrophy

NCT ID: NCT02122952 Completed - Clinical trials for Spinal Muscular Atrophy 1

Gene Transfer Clinical Trial for Spinal Muscular Atrophy Type 1

Start date: May 5, 2014
Phase: Phase 1
Study type: Interventional

The purpose of this trial is to evaluate safety and efficacy of intravenous delivery of AVXS-101 as a treatment of spinal muscular atrophy Type 1 (SMN1).

NCT ID: NCT02080936 Completed - COPD Clinical Trials

Does Muscle Wasting Always Mean Muscle Weakness? A Prevalence Study in COPD

M2W
Start date: January 2014
Phase: N/A
Study type: Observational

Peripheral muscle mass and strength are relevant indicators of COPD survival. Current guidelines recommend to assess muscle strength only in muscle wasted patients. However, a recent study reported quadriceps weakness without muscle wasting (Menon, M et al. Resp. Res.2012, 13:119). Thus, these guidelines raise the risk to miss out some weak patients. In clinical settings, fat-free-mass index (FFMI) is indicated as a simple index to assess muscle wasting. We aimed at determining the prevalence of patients entering in pulmonary rehabilitation (PR) a priori not eligible for muscle strength evaluation given the lack of muscle wasting clinical signs.

NCT ID: NCT02061189 Completed - Clinical trials for Infantile Spinal Muscular Atrophy of Type 2 or 3

Pilot Study of an Innovative Physiotherapy in Patients With Infantile Spinal Muscular Atrophy (SMA)

ExerASI
Start date: March 2014
Phase: N/A
Study type: Interventional

This clinical trial aims to test a new physio-therapeutic approach tailored to type 2 and 3 Spinal Muscular Atrophy patients, based on physical training in swimming-pool. This specific exercise should promote motor skills of trained patients, as we have observed in different mouse models. Patient's motor skills will be assessed using different scales including MFM and Hammersmith. This clinical trial attempts to develop a new non-invasive motor scale with sophisticated instruments. This scale will be useful in future clinical trials on SMA, given the lack of sensitivity of currently available scales. In addition, the study attempts to validate a questionnaire on post-exercise physical well-being.