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Muscular Atrophy clinical trials

View clinical trials related to Muscular Atrophy.

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NCT ID: NCT04228718 Completed - Clinical trials for Spinal Muscular Atrophy

The Burden of Primary Caregivers of Spinal Muscular Atrophy Patients and Their Needs

Start date: July 1, 2019
Phase:
Study type: Observational

The purpose of this study is to assess carer burden, needs, and expectations of Spinal Muscular Atrophy Parents

NCT ID: NCT04199936 Recruiting - Clinical trials for Postoperative Complications

Postoperative Electrical Muscle Stimulation (POEMS)

POEMS
Start date: November 18, 2020
Phase: N/A
Study type: Interventional

Patients lose a significant amount of muscle following major abdominal surgery. This is partly due to a catabolic response to the surgical insult and inflammation, but is also probably due to a lack of muscle use secondary to immobility. This study will aim to assess whether some or even all of postoperative muscle loss in the upper leg muscle group is preventable through electrical muscle stimulation to mimic physical activity.

NCT ID: NCT04199923 Recruiting - Muscular Atrophy Clinical Trials

Mechanisms of Disuse Atrophy in Human Skeletal Muscle (iMOB)

iMOB
Start date: April 1, 2019
Phase: N/A
Study type: Interventional

Loss of muscle can be caused by a variety of stimuli and results in reduced mobility and strength and also impacts whole body health. Whilst it is known that muscles waste the process by which this occurs is not well understood. Furthermore, whilst some muscles waste quickly others seem resistant to the effects of disuse. This study aims to evaluate how quickly changes in muscles start to occur, and investigate the processes which underlie muscle atrophy. By studying muscles which waste quickly and those which are resistant to atrophy this study aims to identify the different processes which lead to muscle loss. This study will also evaluate the differences in muscle changes between young and old people.

NCT ID: NCT04193085 Completed - Clinical trials for Duchenne Muscular Dystrophy

Wearable Technology to Assess Gait Function in SMA and DMD

Start date: November 25, 2019
Phase:
Study type: Observational

The purpose of this project is to devise instrumented insoles capable of accurately measuring gait at each footfall, over multiple hours in any environment. To achieve high accuracy, the investigators will develop a new learning-based calibration framework. Features will be tested in controlled lab settings 39 during a single visit in people with SMA (13), DMD (13) and healthy controls (13) and in 15 participants in real-life environments.

NCT ID: NCT04177134 Recruiting - Clinical trials for Spinal Muscular Atrophy

French Register of Patients With Spinal Muscular Atrophy

SMA
Start date: January 31, 2020
Phase:
Study type: Observational [Patient Registry]

The primary objectives of the study are to obtain clinically meaningful data on survival and outcomes of all the patients with spinal muscular atrophy (SMA) 5q types 1 through 4 (according to international classification), being followed in the reference centers of the disease in France between September 1, 2016 and August 31, 2024. The registry will collect retrospectively and prospectively the longitudinal data of the long-term follow-up for child and adult patients, under real life conditions of current medical practice, in order to document the clinical evolution of patients (survival, motor, respiratory, orthopedic and nutritional), the conditions of use of the treatments, the mortality rates of treated and untreated patients, the tolerance of the treatments, adverse events in order to better define their places in the therapeutic strategy.

NCT ID: NCT04174157 Recruiting - Clinical trials for Spinal Muscular Atrophy (SMA)

Registry of Patients With a Diagnosis of Spinal Muscular Atrophy (SMA)

Start date: September 25, 2018
Phase:
Study type: Observational [Patient Registry]

Spinal muscular atrophy (SMA) is a neurogenetic disorder caused by a loss or mutation in the survival motor neuron 1 gene (SMN1) on chromosome 5q13, which leads to reduced SMN protein levels and a selective dysfunction of motor neurons. SMA is an autosomal recessive, early childhood disease with an incidence of 1:10,000 live births. SMA is the leading cause of infant mortality due to genetic diseases. Until recently, the mainstay of treatment for these patients was supportive medical care. However, advances in medical treatment focusing on gene replacement, gene enhancement, motor neuron protection and muscle enhancement is likely to change the management and prognosis of these patients in the future. The purpose of this registry is to assess the long term outcomes of patients with SMA in the context of advances in treatment options.

NCT ID: NCT04159987 Active, not recruiting - Clinical trials for Spinal Muscular Atrophy

Monitoring to the Evolution of Motor Function in SMA Type II Adults Patients Treated With SPINRAZA®

SMAII
Start date: February 25, 2020
Phase: N/A
Study type: Interventional

SPINRAZA® (Nusinersen) is the first intrathecal administered drug which was approved by the FDA to treat SMA children and adults (2016). The aim is to monitor the evolution of the Motor Function Measure-32 for SMA type II adult patients treated with SPINRAZA® (Nusinersen).

NCT ID: NCT04147741 Completed - Fatigue Clinical Trials

Effects of a Pre-Workout on Performance, Perceptual Responses, Energy Feelings and Muscular Properties, After a Training Microcycle in Adults.

Start date: October 21, 2019
Phase: N/A
Study type: Interventional

The investigation will be conducted as a double blinded, randomized, crossover within-participant comparison design with two 1-week intervention periods separated by 2-weeks for wash out, recovery, period.

NCT ID: NCT04139343 Active, not recruiting - Clinical trials for Spinal Muscular Atrophy

Motor Unit Number Estimation (MUNE) in Adults With Spinal Muscular Atrophy (SMA)

Start date: August 10, 2018
Phase:
Study type: Observational

The primary objective of this research protocol is to study and follow the course of motor neuron loss in individuals with spinal muscular atrophy (SMA) using the electrophysiological technique of motor unit number estimation (MUNE). This study is based on the hypothesis that the electrophysiological technique of motor unit number estimation (MUNE) and compound muscle action potential (CMAP) provide sensitive indicators to assess the severity and progression of disease in adults with SMA.

NCT ID: NCT04131712 Completed - Muscle Atrophy Clinical Trials

Mechanisms Underlying Local and Systemic Effects of Massage

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether massage can attenuate the loss of muscle mass in humans after a short period of disuse.