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Rhabdomyolysis clinical trials

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NCT ID: NCT01022450 Recruiting - Acute Renal Failure Clinical Trials

Study of the Causes of the Breakdown of Muscle Fibers in Hospitalized Patients

Start date: November 2009
Phase: N/A
Study type: Observational

1. Analyze the various causes of breakdown of muscle fibers in hospitalized patients. 2. Analyze the characteristics of these patients in Taiwan (including the drugs history, risk factors and the incidence of complications).

NCT ID: NCT00840112 Terminated - Clinical trials for Peripheral Neuropathy

Vitamin E Treatment for Long-Chain 3-Hydroxyacyl Coenzyme A (CoA) Dehydrogenase (LCHAD) Associated Neuropathy

Start date: July 2010
Phase: N/A
Study type: Interventional

Purpose: People with a genetic defect in the ability to burn fat can also develop a problem with the nerves in their feet. The nerve problem, or neuropathy, can limit their ability to walk. Part of the treatment of their genetic defect in the ability to burn fat is to eat a very low fat diet. Vitamin E is found only in fatty foods like oils and nuts. People with a genetic defect in the ability to burn fat may have low vitamin E because of their low fat diet. The purpose of this study is to test whether vitamin E supplements can improve the nerve function in the feet of people with a genetic defect in the ability to burn fat. Procedures: Blood samples will be drawn at the beginning of the study, after 2 months and after 6 months of vitamin E supplements. The blood will be analyzed for plasma vitamin E concentrations. Around the time of each blood draw subjects will record all the food and beverages he or she consumes for three days. The subject will send the record to the investigator. Subjects will have a physical exam by a doctor specializing in nerves, a neurologist before and after taking vitamin E. They will have nerve function measured with a test called a nerve conduction velocity or NCV. Subjects will be given 800 international units (IU) of vitamin E per day for 6 months.

NCT ID: NCT00654004 Completed - Clinical trials for Trifunctional Protein Deficiency

Fatty Acid Oxidation Disorders & Body Weight Regulation Grant

Start date: April 2006
Phase: N/A
Study type: Observational

Several hormones involved in body weight regulation increase the subject's ability to burn fat for energy. The purpose of this study is to investigate how burning fat for energy may affect those hormones and body weight in children. The study will also determine if eating a diet higher in protein alters the amount of fat you burn and how these hormones control body weight.

NCT ID: NCT00601029 Completed - Clinical trials for Exertional Rhabdomyolysis

Rhabdomyolysis in Basic Training

Start date: January 2008
Phase: N/A
Study type: Observational

The purpose of this study is to: 1. develop a normative database for serum creatine kinase (CK) responses to basic military training (BMT); 2. determine the incidence of exertional rhabdomyolysis (ER) among a large cohort of recruits undergoing BMT; 3. assess the impact of climate on the incidence of ER during BMT; 4. determine the incidence of candidate genes that may be associated with an increased risk of ER.

NCT ID: NCT00592657 Completed - Rhabdomyolysis Clinical Trials

Incidence of Rhabdomyolysis Among Patients Admitted With Jimsonweed Ingestions

Start date: January 2008
Phase: N/A
Study type: Observational

Retrospective chart review to determine the presence of rhabdomyolysis among patients admitted to CHMCA from 1997-2007 with Jimsonweed ingestions and to define possible risk factors predisposing patients to the developement of Jimsonweed-associated rhabdomyolysis.

NCT ID: NCT00549029 Recruiting - Myopathy Clinical Trials

The Association of Genetic Polymorphisms With Statin-Induced Myopathy.

Start date: August 2007
Phase: N/A
Study type: Observational

To observe not only the distribution of single nucleotide polymorphism in genes related with pharmacodynamic and pharmacokinetics alteration of statins but also to analyze the correlation between these SNPs and the incidence of statins-induced myopathy.

NCT ID: NCT00391911 Completed - Rhabdomyolysis Clinical Trials

Study of N-Acetylcysteine (NAC) and Continuous Renal Replacement Therapy (CRRT) for the Treatment of Rhabdomyolysis

Start date: November 2006
Phase: Phase 2
Study type: Interventional

Rhabdomyolysis has many causes including trauma, muscle crush injuries, lack of blood supply to an arm or leg, burns, seizures, drugs and hereditary disorders. Rhabdomyolysis causes the breakdown of muscle cells and the release of a molecule called myoglobin. Myoglobin is very harmful to the kidneys and can lead to kidney failure. Continuous dialysis has been shown to remove the myoglobin molecule from the blood in patients with rhabdomyolysis. N-Acetylcysteine (NAC) has been used in patients receiving contrast dye for x-rays and has shown less worsening of kidney function compared to patients not receiving NAC. Early and aggressive treatment of patients with rhabdomyolysis with standard therapy, continuous dialysis and a drug called N-acetylcysteine (NAC) may prevent the development of acute kidney failure. Patients who develop kidney failure from this disorder are often critically ill and have a much higher chance of not surviving than those who do not develop kidney failure. The purpose of this study is to determine if the use of NAC and Continuous Veno-Venous hemo(dia)filtration (CRRT)early in the course of rhabdomyolysis (in addition to standard therapy)decreases the chance of developing acute renal failure

NCT ID: NCT00241748 Completed - Rhabdomyolysis Clinical Trials

Pharmacoepidemiology and Pharmacogenetics of a Statin Adverse Event

Start date: September 2005
Phase: N/A
Study type: Observational

To conduct a case-control study of factors that increased the risk of rhabdomyolysis, an adverse drug reaction in cerivastatin users