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NCT ID: NCT01803204 Completed - Anxiety Clinical Trials

Patient Education Before Orthognathic Surgery

Start date: February 2013
Phase: N/A
Study type: Interventional

To evaluate the effectiveness in the use of an educational material through: Assessment of knowledge about post-operative orthognathic surgery; assessing levels of anxiety with the survey of Anxiety Inventory-STATE-TRAIT; clinical evaluation of self-care in the management of postoperative signs and symptoms

NCT ID: NCT01802268 Completed - Kidney Transplant Clinical Trials

Planned Conversion From TAC to SRL-based Regimen in de Novo Kidney Transplant Recipients

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

Background Early conversion from calcineurin inhibitor to mammalian target of rapamycin inhibitor is one of the immunosuppressive strategies that have been investigated to mitigate long-term CNi associated adverse events. This study aims to evaluate the conversion from tacrolimus to sirolimus in de novo kidney transplant recipients. This multicenter, open-label study, planned to enroll 297 patients initially treated with tacrolimus, enteric-coated mycophenolate sodium (1440 mg/day, orally) and prednisone. The primary objective is to show superior glomerular filtration rate in the SRL group at 24 months after transplantation.

NCT ID: NCT01801566 Completed - Mouth, Edentulous Clinical Trials

Effectiveness of the Single Implant-retained Mandibular Overdenture Treatment

SIOver
Start date: April 2013
Phase: N/A
Study type: Interventional

This study aims to evaluate the treatment with single implant overdenture for the edentulous mandible. The investigators hypothesize that treatment with lower overdenture retained by a single implant appears to have satisfactory effectiveness as a treatment for patients with specific conditions (such as maladaptive patients), with the advantages of simplicity and greater immediate benefits when compared to the conventional full denture, improving the retention and stability of the denture and better oral-related quality of life.

NCT ID: NCT01800708 Completed - Cataract Clinical Trials

Cataract Surgery With Intracameral Triamcinolone in Infants

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

The aim of the present study is to investigate the outcomes of congenital cataract surgery when injecting intraoperative intracameral triamcinolone versus the postoperative use of oral prednisolone. This is a prospective, randomized clinical trial. Sixty children will be submitted to congenital cataract surgery younger than 2 years of age. They will be randomly divided in two groups. The study group will receive an intraoperative intracameral triamcinolone acetonide injection. The control group will receive prednisolone syrup postoperatively. The surgical outcomes will be assessed after one year.

NCT ID: NCT01799993 Completed - Clinical trials for Pneumonia, Bacterial

Inhaled Amikacin Solution BAY41-6551 as Adjunctive Therapy in the Treatment of Gram-Negative Pneumonia

INHALE 1
Start date: April 13, 2013
Phase: Phase 3
Study type: Interventional

To demonstrate that as adjunctive therapy to intravenous (IV) antibiotics, BAY 41-6551 400 mg (amikacin as free base) administered as an aerosol by the Pulmonary Drug Delivery System (PDDS) Clinical every 12 hours is safe and more effective than placebo (aerosolized normal saline) administered as an aerosol by the PDDS Clinical every 12 hours, in intubated and mechanically-ventilated patients with Gram-negative Pneumonia. The secondary endpoint objectives are to evaluate the superiority of aerosolized BAY 41-6551 versus aerosolized placebo in pneumonia-related mortality, the Early Clinical Response at Day 10, the days on ventilation, and the days in the intensive care unit (ICU).

NCT ID: NCT01799863 Completed - Clinical trials for Conjunctivitis, Viral

Artificial Tears Versus Preservative Free Ketorolac Trometamol 0.45% for Acute Viral Conjunctivitis

Start date: June 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the evolution of the symptoms of acute viral conjunctivitis using preservative free ketorolac trometamol 0.45% associated with carboxymethylcellulose compared with isolated use of preservative-free artificial tears.

NCT ID: NCT01798342 Completed - Clinical trials for Pulmonary Aspiration of Gastric Contents

Safety of Gastric Volume Emptying After the Intake of Maltodextrin and Glutamine

Start date: March 2012
Phase: Phase 2
Study type: Interventional

Carbohydrates (CHO)-based drinks 2h before the induction of anesthesia are recommended to decrease insulin resistance. The addition of glutamine (GLN) in these beverages may enhance the benefits of CHO alone. However, only a few studies tested the safety of this formula. The objective of this study was to evaluate the gastric residual volume (GRV) after the intake of a beverage containing CHO plus GLN using magnetic resonance (MRI).

NCT ID: NCT01796392 Completed - Emphysema Clinical Trials

Pulmonx Endobronchial Valves Used in Treatment of Emphysema (LIBERATE Study)

LIBERATE
Start date: July 2013
Phase: N/A
Study type: Interventional

The purpose of this research is to study an investigational medical device that is designed to produce lung volume reduction in diseased areas of the lungs in patients with severe emphysema.

NCT ID: NCT01795222 Completed - Clinical trials for Early Childhood Caries

Midazolam Efficacy for Sedating Preschoolers Undergoing Dental Treatment

Pedsed-I
Start date: March 2012
Phase: Phase 4
Study type: Interventional

Evaluation of oral midazolam to improve children's behavior and reduces the stress and anxiety during dental treatment

NCT ID: NCT01794910 Completed - Clinical trials for Pelvic Floor Muscle Weakness

A Randomized Controlled Trial Comparing the Effect of Pelvic Floor Muscle Training

PFMT
Start date: February 2010
Phase: N/A
Study type: Interventional

Aim: To determine the effects of pelvic floor muscle training (PFMT) in women with a single delivery route. Pregnancy and delivery route alter the pelvic floor muscle strength and are considered risk factors for urinary incontinence and genital dystopias. Methods: A Randomized controlled clinical trial with two hundred ninety-seven women aged 35 to 45 years old were selected for functional assessments of their pelvic floors by vaginal digital palpation and perineometry. One hundred sixty-five (69.7%) exhibited muscle strength deficits and were included in the clinical trial. The participants were distributed into two groups based on the delivery route (A, vaginal delivery and B, cesarean delivery) and were then randomly subdivided into Groups A1 (n = 44) and B1 (n = 42), who performed PFMT, and Groups A2 (n = 39) and B2 (n = 40), who did not undergo muscle training. The PFMT involved perineal contraction exercises in the dorsal decubitus, sitting, and standing positions and was applied twice per week for a total of 15 sessions. The functional assessment of pelvic floor by vaginal digital palpation and perineometry was performed after 15 sessions of pelvic´s floor muscles training. The statistical analysis was performed using the Mann-Whitney and Z tests at a 5% level of significance.