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NCT ID: NCT02143453 Completed - Obesity Clinical Trials

Comparative Study of High Intensity Interval Training and Endurance Training in Juvenile Obesity

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

Exercise is an effective strategy to manage juvenile obesity; however this ideal exercise training mode is still unclear. In this study, the investigators compared the health-related effects of high intensity interval training versus endurance training in obese children.

NCT ID: NCT02142179 Completed - Asthma Clinical Trials

Impact of a Curriculum Intervention on Asthma Knowledge in Adolescents of a Public School in Salvador-Bahia-Brazil

KARE
Start date: November 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to estimate the impact of a curriculum intervention on asthma knowledge in adolescents of a public school in Salvador-Bahia-Brazil.

NCT ID: NCT02139735 Completed - Clinical trials for Temporomandibular Joint Disorders

Therapeutic Response of Ultrasound and Muscular Stretching in Temporomandibular Disorder Patients

Start date: March 2012
Phase: N/A
Study type: Interventional

The combination of ultrasound and muscular stretching may have positive effects on pain relief and on the balance of the masticatory muscles activity.

NCT ID: NCT02139631 Completed - Clinical trials for Haemodynamic Rebound

Hemodynamic Repercussions of Noninvasive Ventilation

Start date: May 2014
Phase: N/A
Study type: Interventional

The noninvasive ventilation (NIV) is a method of ventilatory support that does not require artificial airway. Its application is associated with complex hemodynamic repercussions, therefore is important to identify them for safety and effectiveness of the technique application. The main objective of this research is to evaluate the hemodynamic repercussions using doppler echocardiography in healthy volunteers submitted a different values of positive end expiratory pressure (PEEP) by the following ventilatory modes: Continuous positive airway pressure (CPAP) and Bilevel. The study hypothesis is that the positive end expiratory pressure (PEEP) may cause hemodynamic repercussions as: reduction of the ventricles pre-load, left ventricle after load, cardiac output and reduction in the diameter of the superior vena cava, due to the increase in the intrathoracic pressure and pulmonary volumes.

NCT ID: NCT02139306 Completed - Cystic Fibrosis Clinical Trials

Study of Ataluren in Nonsense Mutation Cystic Fibrosis (ACT CF)

Start date: August 2014
Phase: Phase 3
Study type: Interventional

This is a Phase 3, international, multicenter, randomized, double-blind, placebo-controlled, efficacy and safety study of ataluren in patients with nonsense mutation cystic fibrosis (nmCF) not receiving chronic inhaled aminoglycosides.

NCT ID: NCT02138058 Completed - Compulsive Shopping Clinical Trials

Topiramate Trial for Compulsive Buying

TFO
Start date: January 2015
Phase: Phase 2
Study type: Interventional

It is a double blind controlled study to test the hypothesis that Topiramate is more effective than placebo in the treatment of compulsive buying, during a period of 12 weeks

NCT ID: NCT02136134 Completed - Multiple Myeloma Clinical Trials

Addition of Daratumumab to Combination of Bortezomib and Dexamethasone in Participants With Relapsed or Refractory Multiple Myeloma

Start date: August 15, 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the effects of administration of daratumumab when combined with VELCADE (bortezomib) and dexamethasone compared with bortezomib and dexamethasone alone, for participants with relapsed or refractory multiple myeloma.

NCT ID: NCT02135471 Completed - Gingival Recession Clinical Trials

Root Coverage in Smokers With Acellular Dermal Matrix Graft and Enamel Matrix Derivative

Start date: June 2009
Phase: Phase 2
Study type: Interventional

Smoking has a negative effect on the predictability and stability of root coverage procedures because of decreased blood supply and fibroblast activity. Long-term evaluation of this procedure in smokers is important for clinical decision making, because it provides information about the stability of results over time. In smokers, enamel matrix derivative (EMD) used at acellular dermal matrix graft (ADMG)/ soft tissue interface could be an alternative to improve the deficient healing potential, since EMD has the capability of stimulating angiogenesis. At the ADMG/ root surface interface, it could improve the deficient fibroblast activity in smokers and therefore reduce the presence of a long junctional epithelium. The aim of this randomised controlled clinical study was to investigate whether EMD contributes to the root coverage of gingival recessions performed with ADMG in smokers during a 12-month follow-up. Twenty smokers with bilateral Miller Class I or II gingival recessions ≥ 3 mm will be selected. The test group will be treated with an association of ADMG and EMD, and the control group with ADMG alone. Some clinical parameters as: probing depth, relative clinical attachment level, gingival recession height, gingival recession width, keratinized tissue width and keratinized tissue thickness will be evaluated before surgery and after twelve months.

NCT ID: NCT02134743 Completed - Clinical trials for Dental Implant Failed

Evaluation of the Stability of Implants With Two Different Surface Treatments

Start date: April 2014
Phase: N/A
Study type: Interventional

The aim of this study is to compare the stability of dental implant surface treated by sandblasting abrasive particles and acid subtraction (Control) with hydrophilic surfaces dental implants (chemical) and with a higher surface energy (Test) for a period of 16 weeks after installation. The evaluation will be made by analyzing the resonance frequency (Ostell). The hypothesis to be tested will be that implants with hydrophilic surface show increased secondary stability prior to the implants treated by acid etching.

NCT ID: NCT02134626 Completed - Liver Cirrhosis Clinical Trials

Simvastatin Effect on Portal Hypertension

Start date: August 2010
Phase: Phase 3
Study type: Interventional

It´s a clinical research of the effects in portal hypertension caused by simvastatin. We are going to use the hepatic venous pressure gradient(HVPG) measurement and the azygos flow at echoendoscopy to evaluate the benefits of the drug. Preliminary studies demonstrated that simvastatin can lower portal pressure.