Clinical Trials Logo

Filter by:
NCT ID: NCT00884429 Completed - Viral Bronchiolitis Clinical Trials

Effectiveness of Chest Physiotherapy in Infants With Acute Viral Bronchiolitis

ECPAVB
Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to verify the effectiveness of chest physiotherapy (actual versus conventional) on respiratory distress in infants with acute viral bronchiolitis.

NCT ID: NCT00883493 Completed - Clinical trials for Acute Bipolar Depression

Efficacy and Safety of Quetiapine Versus Quetiapine Plus Lithium in Bipolar Depression

QUALITY
Start date: April 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy of quetiapine fumarate monotherapy with quetiapine fumarate in combination with lithium in the treatment of a major depressive episode in patients with bipolar disorder.

NCT ID: NCT00883376 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome

Classification of Stanford for Snore as Factor of Aggravation of the Apnea Hypopnea Index (AIH) in Patients With Obstructive Sleep Apnea Syndrome (OSAS)

StanforAIH
Start date: January 2007
Phase: N/A
Study type: Observational

Introduction: Obstructive sleep apnea syndrome (OSAS) became an important and prevalent illness in recent years. The population occidental becomes fat each time, and this symptom is associated the biggest risk for the OSAS. Snore presence is extremely associated with OSAS. Snoring is present in about 90 - 95% of the patients with OSAS. Objectives: Evaluate the influence in the Stanford classification as predictor factor of gravity of the OSAS. Materials and Methods: They evaluated and classified 107 patients, Classification of Mallampati, Friedman, Classification of Stanford and how much the gravity of the OSAS for the AIH.

NCT ID: NCT00883025 Completed - Clinical trials for Obstructive Sleep Apnea Syndrome

Correlation Between Friedman Classification and the Apnea Hypopnea Index (AIH) in a Population With Obstructive Sleep Apnea Syndrome (OSAS)

FriedmAIH
Start date: February 2007
Phase: N/A
Study type: Observational

Introduction: OSAS is an important disease in the actual medic scene. It is important for correlation with chronic cardiovascular disease that leaves an increase in morbimortality and socioeconomic disability to patients with apnea. Objectives: Determinate the correlation between Friedman Classification and the obstructive sleep apnea syndrome (OSAS) gravity through AHI (Apnea Hypopnea Index) in patients with OSAS for surgical indication and evaluation. Materials and Methods: The investigators evaluated and classified 84 patients, in the scale of Epworth, Friedman and how much the gravity of the SAHOS for the AHI.

NCT ID: NCT00882921 Completed - Hunter Syndrome Clinical Trials

An Observational Study Evaluating Anti-Idursulfase Serum Antibody Response in Hunter Syndrome Patients

Start date: October 14, 2008
Phase:
Study type: Observational

The objective of this study is to evaluate the effect of anti-idursulfase antibodies on idursulfase safety (measured by infusion related adverse events) between patients who develop anti-idursulfase antibodies and patients who do not after long-term idursulfase enzyme replacement therapy (ERT).

NCT ID: NCT00881699 Completed - HIV Infections Clinical Trials

Testing an HIV Prevention Intervention for Psychiatric Patients in Brazil

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

This study will test the effectiveness of a program aimed at reducing behaviors that increase HIV risk among people with severe mental illnesses.

NCT ID: NCT00881543 Completed - Diabetes Type 2 Clinical Trials

"Effect of Dipeptidyl Peptidase IV After Diets in näive Type 2 Diabetic Patients"

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

The purpose of this study is to demonstrate the secretion of glucose, insulin, glucagon, C-peptide and lipid profile after isocaloric diets with different nutritional compounds (fat, protein and carbohydrate food) in drug näive tipo 2 patients.

NCT ID: NCT00881374 Completed - Hygiene Clinical Trials

Dermacyd Infantile (Lactic Acid)- Compatibility.

Start date: February 2009
Phase: Phase 4
Study type: Interventional

Primary Objective: To demonstrate the absence of irritation potential (primary dermic irritability and cumulated dermic irritability) and allergic potential (sensibilization) of the product Dermacyd Infantile.

NCT ID: NCT00881348 Completed - Hygiene Clinical Trials

Dermacyd Infantile (Lactic Acid) - Photo Evaluation.

Start date: February 2009
Phase: Phase 4
Study type: Interventional

Primary Objective: To demonstrate the absence of photo irritation and photosensitization potential of the product Dermacyd Infantile (Lactic Acid).

NCT ID: NCT00881270 Completed - Hygiene Clinical Trials

Dermacyd Infantile - Acceptability.

Start date: March 2009
Phase: Phase 4
Study type: Interventional

Primary Objective: To prove the safety of the formulation in normal conditions of use.