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Muscle Weakness clinical trials

View clinical trials related to Muscle Weakness.

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NCT ID: NCT01727193 Completed - Myasthenia Gravis Clinical Trials

The Efficacy and Safety of Leflunomide or Azathioprine Therapy in Myasthenia Gravis Patients After Expand Thymectomy

Start date: September 2012
Phase: Phase 3
Study type: Interventional

This is a randomized controlled clinical study. The investigators screen of eligible patients, randomized divide into the following two groups: corticosteroids + azathioprine group, corticosteroids + leflunomide group. The investigators treat the enrolled patients, estimate efficacy and observed the side effects according to the requirements of program. The investigators establish a clinical database for recording patients date and statistical analysis. Evaluation of short-term and long-term efficacy of thymectomized myasthenia gravis patients in the different group prove that what kind of treatment can improve the cure rate. The investigators will evaluate the acute toxicity (gastrointestinal side effects, liver and kidney dysfunction) and long-term toxicity (immune dysfunction, gonadal suppression) when the investigators apply these therapy in the treatment of different clinical types of myasthenia gravis.

NCT ID: NCT01721434 Recruiting - Weaning Failure Clinical Trials

Effects of Levosimendan on Diaphragm Function in Mechanically Ventilated Patients

Start date: September 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Levosimendan is a relatively new drug that improves cardiac contractility in patients with heart failure. Its main mechanism of action is enhanced binding of calcium to the myocardial contractile proteins. Recent data from our lab showed that levosimendan improves contractility of human diaphragm in vitro (muscle fibers from COPD patient diaphragm) and in vivo (healthy subjects). Accordingly, levosimendan may appear of value in the treatment of disorders associated with impaired respiratory muscle function, such as mechanically ventilated patients.We hypothesize that levosimendan could improve respiratory muscle function in mechanically ventilated patients commencing a CPAP trial.

NCT ID: NCT01704976 Completed - Muscle Weakness Clinical Trials

SR-WBV Training for Frail Elderly in the Skilling up Stage

Start date: September 2012
Phase: N/A
Study type: Interventional

This randomized controlled study aims to examine long term effects in the skilling up phase over 4 weeks on physical functional performance and strength of mechanical SR-WBV and dance therapy intervention in a frail elderly population.

NCT ID: NCT01679977 Completed - Clinical trials for Muscle Weakness Condition

Vibrational-proprioceptive Resistance Exercise Training Versus Neuromuscular Electrical Stimulation Training in Elderly People With Muscle Weakness

MOBIL
Start date: June 2008
Phase: N/A
Study type: Interventional

Study the structural behaviours of weak muscle of elderly and evaluate the efficiency of two different types of training.

NCT ID: NCT01655277 Completed - Fall Risk Clinical Trials

Ultrasound Guided Adductor Canal Block Versus Femoral Nerve Block for Quadriceps Strength and Fall-risk

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

Our objective was to determine if an ultrasound guided ACB can preserve quadriceps strength, thus minimizing weakness of knee extension compared with ultrasound guided femoral nerve block. Our primary outcome was the percent of maximum voluntary isometric contraction (MVIC) of knee extension preserved at 30 mins after either an ACB or FNB. Secondary outcomes included MVIC of knee extension at 60 min, hip adduction at 30 and 60 mins, and assessment of fall risk with the Berg Balance Scale (BBS) at 30 minutes.

NCT ID: NCT01624272 Completed - Muscle Weakness Clinical Trials

Respiratory Muscle Training in Institutionalized Elderly Population

Start date: November 2008
Phase: N/A
Study type: Interventional

The global loss of muscle mass and strength associated with aging is a cause of functional impairment and disability, particularly in the frail elderly. Respiratory function can be severely compromised if there is a decrease of respiratory (RM) strength complicated by the presence of comorbidities and physical immobility. Previous studies have shown that the specific RM training is an effective method to increase RM strength, both in healthy people and patients. In this case, specific RM training may be regarded as a beneficial alternative to improve RM function, and thus prevent physical and clinical deterioration in this population. The hypothesis is that specific RM training would improve RM strength and endurance in the experimental groups vs. control who do not participate in RM training. Institutionalized elderly people with an inability to walk were randomly allocated to a control group, a Threshold group or a Pranayama group. Both experimental groups performed a supervised RM training, five days a week for six consecutive weeks. The maximum inspiratory and expiratory pressures (MIP and MEP) and the maximum voluntary ventilation (MVV) were assessed at four time points in each of three groups.

NCT ID: NCT01604408 Completed - Muscle Weakness Clinical Trials

A Study in Older Participants Who Have Fallen and Have Muscle Weakness

Start date: May 2012
Phase: Phase 2
Study type: Interventional

LY2495655 is an investigational drug being tested for muscle wasting.

NCT ID: NCT01570816 Recruiting - Stroke Clinical Trials

Improving Ambulatory Community Access After Paralysis

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

The purpose of this research study is to evaluate the effectiveness of functional electrical stimulation (FES) provided by an implanted pulse generator (IPG) in correcting hip, knee and ankle function to improve walking in people with partial paralysis.

NCT ID: NCT01549847 Withdrawn - Clinical trials for Postpoliomyelitis Syndrome

A Randomized, Double Blind, Placebo Controlled Trial L-carnitine and Piracetam in the Treatment of Weakness, Muscle Fatigue and Muscle Pain in the Postpoliomyelitis Syndrome

Start date: n/a
Phase: Phase 3
Study type: Interventional

This protocol aims to assess of L-carnitine and piracetam to relieve weakness, muscle fatigue and muscle pain in patients with Postpoliomyelitis Syndrome.

NCT ID: NCT01536327 Withdrawn - Muscle Weakness Clinical Trials

Biomarker for Metachromatic Leukodystrophy (BioMeta) Disease

BioMeta
Start date: August 20, 2018
Phase:
Study type: Observational

Development of a new MS-based biomarker for the early and sensitive diagnosis of Metachromatic Leu-kodystrophy disease from blood (plasma)