Clinical Trials Logo

Filter by:
NCT ID: NCT00929890 Active, not recruiting - Obesity Clinical Trials

Additional Metabolic and Vascular Effects of Exercise in Patients on Diet-based Weight Loss Programs

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

This study tests the hypothesis that exercise training can confer additional benefit to patients in weight-loss programs in the form of improvements in either metabolic or vascular parameters or both. Patients will be randomized to either diet plus conventional physical activity or diet plus a planned exercise training. The interventions will be carried out until the patients lose between 5% and 7.5% of their initial weight. At entry and at the end, all subjects will be evaluated for outcomes such as blood glucose, lipid profile, insulin, c-reactive protein, fibrinogen, vascular reactivity (doppler ultrasound) and total and abdominal visceral fat (CT-scan). Both groups will be compared.

NCT ID: NCT00926315 Active, not recruiting - Breast Neoplasms Clinical Trials

Gene Expression Profile of Breast Cancer Samples After Vitamin D Supplementation

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

The purpose of this study is to evaluate whether calcitriol supplementation may reduce tumor cell proliferation and influence gene expression profile of breast cancer samples from post-menopausal patients.

NCT ID: NCT00925158 Active, not recruiting - Aging Clinical Trials

Dissector Assisted Malar Elevation for Rhytidoplasty

DAME
Start date: December 2007
Phase: N/A
Study type: Interventional

BACKGROUND: Endoscopy was first used in plastic surgery for the treatment of frontal rhytides. This minimally invasive approach allows the treatment of frontal wrinkles using a practical procedure that does not directly interfere with the frontalis muscle, acting only on its antagonists. It is also possible to treat the middle third of the face, but these evolutions depends on special surgical instruments. Videoendoscopic approach in rhytidoplasty have been improved by new devices and surgical instruments. The mid third of the face can be treated in different ways. Zygomatic projection can be achieved by the use of the Dissector Assisted Malar Elevation (DAME) procedure. AIM: Evaluate the zygomatic projection achieved by DAME in videoendoscopic rhytidoplasties. METHODS: 30 non-white female patients, 30 to 59 years old, will be submitted to videoendoscopic rhytidoplasty with malar elevation by the DAME. Pre- and post-operative facial appearance will be evaluated by digital photogrammetry.

NCT ID: NCT00914472 Active, not recruiting - Thrombus Clinical Trials

Comparison of Two Heparin Formulations in Patients With Chronic Renal Failure.

HEPHIP0509
Start date: April 2010
Phase: Phase 3
Study type: Interventional

Investigate, through a randomized, open, parallel and comparative, non-inferiority of heparin sodium produced by laboratory Hipolabor compared to heparin manufactured by APP in patients on hemodialysis due to renal failure, through the control of hemostasis, verified by formation of clot (fibrin) in the hemodialysis system and pharmacodynamic parameters (TTPA and Anti-Xa) during the use of heparin

NCT ID: NCT00894621 Active, not recruiting - Clinical trials for Mechanical Ventilation

Norepinephrine as Early Vasopressor Therapy in Children Undergoing Mechanical Ventilation

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

The purpose of this study is to assess the effectiveness from early infusion of norepinephrine in pediatric patients submitted to mechanical ventilation for the use of sedative and analgesics drugs.

NCT ID: NCT00889551 Active, not recruiting - Pregnancy Clinical Trials

Pregnancy and Growth of Adolescent Mothers and Their Child

Start date: n/a
Phase: N/A
Study type: Observational

This study intends to observe the epidemiology of pregnancy and growth of adolescent mothers and their child in their first year on the development and growth ambulatory at Brasilia University Hospital (HUB). The study hypothesis is that adolescent growth is disturbed by a pregnancy in this age. Another hypothesis is that their child's growth and development could be obstructed.

NCT ID: NCT00887952 Active, not recruiting - Dental Caries Clinical Trials

Partial Removal of Caries Dentines

PRCD
Start date: August 2005
Phase: N/A
Study type: Interventional

The aim of this multicenter randomized controlled clinical trial is to evaluate the effectiveness of an alternative treatment for deep caries lesions in Public Health Services. The alternative treatment consists of partial removal of carious dentine followed by restoration. The subjects were assigned to test or control groups: test - carious dentine partial removal and restoration in one session, and control - stepwise excavation. The stepwise excavation consists of partial removal of carious tissue from the cavity floor, indirect pulp capping with calcium hydroxide cement; temporary filling; cavity re-opening after 60 days, removal of the remaining soft carious tissue and filling. Each group was divided according to the filling material: amalgam or resin. The radiological exams are being performed before and after the treatment and then annually. Clinical evaluation of the restorations is performed right after the treatment and then annually (modified USPHS System). All evaluations are performed by calibrated and trained dentists.

NCT ID: NCT00879372 Active, not recruiting - Bipolar Disorder Clinical Trials

Efficacy of Adjunctive Tianeptine in the Treatment of Bipolar Depression

Start date: March 2009
Phase: Phase 3
Study type: Interventional

One of the main challenges in the treatment of Bipolar Disorder (BD) is to achieve better functioning outcomes after syndromal recovery. Even treatment-responsive patients, who remain symptomatically well for extended periods of time, frequently demonstrate sub-threshold symptoms and continuing psychosocial morbidity and cognitive impairment. The cognitive impairment that persists during interepisode periods stands out as a major correlate of functional impairment, and may be a core aspect of the BD pathophysiology. In this context, tianeptine stands out as a therapeutic agent with unique properties, which match most of the conditions found in BD. This is an enriched maintenance study of the use of tianeptine as an adjunctive therapy in bipolar depression. All participants will receive tianeptine in an open label manner for a period of two months, following which they will be assigned randomly to the treatment with tianeptine or placebo in a double-blind fashion for six months. All patients will remain on treatment as usual for the duration of the trial. Along with clinical response, the investigators will prospectively evaluate the improvement in working and declarative memory, two cognitive prefrontal- and hippocampus-dependent processes, respectively, and the effects of tianeptine on serum BDNF levels.

NCT ID: NCT00865540 Active, not recruiting - Cataract Clinical Trials

Effect of Anti-inflammatory Topical Prednisolone, Nepafenac and Ketorolac in Intra-operative Mydriasis in Facetectomies

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

The main objective of this study is to compare the effect of preoperative use of anti-inflammatory topical prednisolone acetate 1%, nepafenac 0.1% and ketorolac tromethamine 0.4% of, plus a placebo, in maintaining the intra-operative mydriasis in extraction.

NCT ID: NCT00861562 Active, not recruiting - Hemorrhoids Clinical Trials

Clinical Efficacy and Safety Evaluation of the Drug Imescard Compound Water Smartweed Pills

Start date: April 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study was to assess the clinical efficacy and safety of the drug Imescard water smartweed compound pills in the treatment of patients with chronic constipation and hemorrhoidal disease.