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NCT ID: NCT00985803 Enrolling by invitation - Clinical trials for Systemic Lupus Erythematosus

Physical Activity in Patients With Systemic Lupus Erythematosus

LESPA
Start date: November 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to check the improvement in quality of life in patients with systemic lupus incorporated into a routine of physical activity. Randomized controlled blinded trial, 63 patients aged 42.9 ± 14.4 and diagnosis of systemic lupus erythematosus (SLE) according to the criteria of the College American Rheumatology, 1997. After randomization patients were allocated into 3 groups, control group (CG) (n = 21), training cardiovascular (CT) (n = 20), resistance training (RT) (n = 22), performing 12 weeks of intervention with a frequency of three times weeks and were evaluated at two different times (T0 and T12). As primary outcome quality of life was assessed by the inventory Generic Assessment of quality of life by the Medical Outcomes Study 36 -- Healthy ItemShort Form Survey (SF36) and as secondary outcomes functional capacity evaluation of pain symptoms (visual scale analogue pain [VAS]), intensity of symptoms of depression (Beck Depression Inventory [BDI]), index of disease activity (Systemic Lupus Disease Activity Inventory Erythmatodud [SLEDAI]), capacity aerobic (walking test of 12 minutes [T12]), subjective perception effort (subjective scale of Borg [Borg]), limb muscle strength lower (analog dynamometer [strength]), electrical activity member lower (surface electromyography [EMG]), amount of products (inventory amount of Medicines).

NCT ID: NCT00969930 Enrolling by invitation - Bipolar Clinical Trials

Genetic Association Study Between Single Nucleotide Polymorphisms (SNPs) and Cognitive Performance in Young Bipolar Type I Patients: LICAVALGENE

Licavalgene
Start date: August 2009
Phase: N/A
Study type: Observational

This is a genetic association study of cognitive impairment in young bipolar disease type I patients without medications in mania, depression, hypomania or mixed states.

NCT ID: NCT00896831 Enrolling by invitation - Clinical trials for Hepatic Encephalopathy

Therapeutic Efficacy of Oral L-Ornithine-L-Aspartate on Minimal Encephalopathy

PORTOALEGRE
Start date: November 2008
Phase: Phase 4
Study type: Interventional

The study aimed to assess the effectiveness and safety of L-ornithine-L-aspartate in the management of hepatic encephalopathy.

NCT ID: NCT00852800 Enrolling by invitation - Renal Impairment Clinical Trials

Low-dose Albumin Solution in SBP: a Randomized Double-blind Pilot Study

ALTERNATE
Start date: March 2006
Phase: Phase 2
Study type: Interventional

Spontaneous bacterial peritonitis (SBP) is a common and severe complication of cirrhosis. The most serious complication of SBP is the hepatorenal syndrome (HRS), which occurs in up to 30 percent of patients, with high mortality. Intravenous albumin (1.5 g/kg at diagnosis and 1 g/kg 48 hours later - standard regimen) helps to prevent HRS and improves survival. No information exists on the efficacy of lower doses of albumin. This study was designed to allow direct comparison among different doses of intravenous albumin in patients with SBP - standard (SR) vs dose reduced regimen (DRR) - in order to prevent renal failure and mortality.

NCT ID: NCT00825552 Enrolling by invitation - Clinical trials for Severe Mood Dysregulation

Pharmacological Treatment of Children and Adolescents With Severe Mood Dysregulation

Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether Risperidone is effective in children and adolescents with severe mood dysregulation.

NCT ID: NCT00676325 Enrolling by invitation - Hernia Clinical Trials

Surgical Treatment To Greater Anterior Vaginal Prolapse

Nazcatcâ„¢
Start date: January 2007
Phase: Phase 4
Study type: Interventional

A RCT study to compare traditional colporrhaphy versus polypropylene mesh in treatment of the anterior vaginal wall prolapse.