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NCT ID: NCT01215760 Completed - Clinical trials for Median Nerve Disease

Sensory Reeducation in Peripheral Nerve Injuries of Hand

HandtherRCT
Start date: March 2009
Phase: N/A
Study type: Interventional

Objectives: To develop a protocol for early treatment using sensory reeducation through the mirror after surgical reconstruction of the median nerve and / or ulnar hand, and its comparison with the evolution of the return of skin sensitivity after a not early rehabilitation which will be conducted by physiotherapists, with blinding of the evaluators.

NCT ID: NCT01215708 Active, not recruiting - Renal Calculi Clinical Trials

Effects of the Use of Adjuvant Drugs After Extracorporeal Shockwave Lithotripsy (ESWL) in Renal Calculus

Start date: August 2006
Phase: Phase 3
Study type: Interventional

The investigators objective is to study if some drugs can improve the success rate of extracorporeal shockwave lithotripsy for renal stones.

NCT ID: NCT01213875 Completed - Heart Failure Clinical Trials

A Multifaceted Nurse-based Strategy Reduces HEart FaiLure Morbidity in PatiENts Admitted for Acute Decompensated Heart Failure in Brazil

HELEN II
Start date: August 2009
Phase: N/A
Study type: Interventional

The home based intervention is a multidisciplinary approach that has shown benefit in the follow-up of patients with Heart Failure (HF). It is considered one of the most effective approaches and humanized by education and care for the patient in his environment of routine. In this study the monitoring of HF patients in the home after hospital discharge will include the reinforcement, monitoring and reassessment of previously provided guidance on the disease and self-care, compliance to prescribed medications and especially the early recognition of signs and symptoms of decompensation by patients and their caregivers.

NCT ID: NCT01213719 Completed - Healthy Subjects Clinical Trials

Effects of Betaine Supplementation on Strength and Muscle Creatine Content

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

It has been suggested that betaine supplementation may improve muscle strength by increasing muscle creatine content. However, there is no data supporting this assumption. The investigators speculate that betaine supplementation could enhance intramuscular creatine content, which would result in strength improvements.

NCT ID: NCT01212835 Terminated - Morbid Obesity Clinical Trials

Effect of RING on Gastroesophageal Reflux (GERD) After RYGBP

RING
Start date: October 2010
Phase: N/A
Study type: Interventional

Silastic rings have been used around the gastric pouch in order to promote better weight loss after Roux-and-Y gastric bypass surgery ( RYGBP). However the investigators have shown that some patients developed gastroesophageal reflux disease after RYGBP in a previous study. The investigators hypothesized that the use of a silastic ring may play a role in promoting GERD after this operation.

NCT ID: NCT01211873 Completed - Clinical trials for Central Nervous System Diseases

Safety and Efficacy Evaluation of DOTAREM® in MRI of Central Nervous System (CNS) Lesions

SENTIO
Start date: September 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to look at the safety (what are the side effects)and efficacy (how well does it work) of Dotarem® when used in taking images of the brain / spine. The results will be compared to the results of MRI taken without Dotarem.

NCT ID: NCT01211769 Completed - Alcohol Dependence Clinical Trials

Effects of Omegas 3 and 6 on Alcohol Dependence

Start date: February 2006
Phase: Phase 3
Study type: Interventional

Context: The treatment of alcoholism is a challenge for psychiatrists and patients. Some studies have shown that alcohol alters the environment of the membranes, mainly by modifying their permeability through the lipid fraction. These lipids are known as essential fatty acids (EFA) because they are obtained only through the diet, as the human body is unable to synthesize them. Linolenic acid (LA), or omega 6, and alpha-linolenic acid (ALA), or omega 3, are polyunsaturated fatty acids (PUFAs). Finally, ethanol changes the absorption and metabolism of PUFAs, and it's supplementation may be helpful for alcohol dependence recovery. Objective: to assess the effectiveness of PUFAs supplementation in the treatment of alcohol dependent patients.

NCT ID: NCT01210703 Active, not recruiting - Clinical trials for Obstructive Sleep Apnea Syndrome

Acoustic Pharyngometry in Obstructive Sleep Apnea Syndrome Patients, With Indication of Continuous Positive Air Pressure

APOSAS
Start date: May 2009
Phase: N/A
Study type: Observational

Acoustic Pharyngometry (AP) is a method of measurement of Transversal Sectional Areas (TSA) and Volumes of oral cavity and pharynx, based on acoustic waves. The aim of this study is to describe changes on oropharynx dimensions caused by CPAP (Continuous Positive Air Pressure) in patients with severe Obstructive Sleep Apnea Syndrome when compared with patients with Primary Snore, using AP. The exam will be made during the use of CPAP, at various pressures. The investigators also intend to determine if pressure determined by Polysomnography in OSAS patients cause some type of different change in AP graphic.

NCT ID: NCT01210469 Completed - Osteoporosis Clinical Trials

Effectiveness of Two Treatments on Posture and Balance in Elderly Women With Osteoporosis

Start date: July 2007
Phase: N/A
Study type: Interventional

The purpose of this study was compare the efficacy of two exercise programs - the first consisting of balance training and muscle strength and the second consisting of balance training and muscle stretching exercises - to improve postural control in elderly women with osteoporosis.

NCT ID: NCT01210365 Terminated - Clinical trials for Congestive Heart Failure

Safety and Efficacy of Furosemide 40mg + Amiloride Hydrochloride 10mg to Reduct Edema

Start date: January 1, 2011
Phase: Phase 3
Study type: Interventional

The study consists in two treatment groups, one group will receive Diurisa® (furosemide 40 mg + amiloride chloride 10 mg) and the other one will receive furosemide 40 mg (Lasix®)