Clinical Trials Logo

Filter by:
NCT ID: NCT01217606 Completed - Ocular Hypertension Clinical Trials

Safety and Efficacy of Triple Combination Therapy in Patients With Primary Open-Angle Glaucoma or Ocular Hypertension

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

This study will evaluate the safety and efficacy of Triple Combination Therapy compared with Fixed Combination brimonidine tartrate/timolol ophthalmic solution in patients with primary open-angle glaucoma or ocular hypertension.

NCT ID: NCT01217255 Completed - Hemophilia A Clinical Trials

Comparing the Burden of Illness of Hemophilia in the Developing and the Developed World

Start date: September 2010
Phase:
Study type: Observational

Because of high cost, persons with hemophilia in many developing countries cannot afford adequate treatment. For example, many persons with hemophilia in India and China are only rarely treated with factor replacement in response to bleeds, and as a result many have developed significant arthropathy and disability. A pilot study in China estimated the mean Hemophilia Joint Health Score (HJHS) at 13.1 (SD 9.03) suggesting that these children had highly prevalent, severe joint disease. The lack of relationship between the HJHS and treatment history suggests overall inadequate therapy. The proposed study will quantify the burden of arthropathy, physical disability, and quality of life (QoL) in boys with hemophilia in Brazil - where comprehensive treatment is just beginning to be widely available. This study will also provide an opportunity to compare these outcomes to those observed in Canada, where the dominant therapy has become life-long prophylaxis.

NCT ID: NCT01217177 Completed - Clinical trials for Locally Advanced Cervical Cancer

A Study of mTOR Inhibitor Everolimus (RAD001) in Association With Cisplatin and Radiotherapy for Locally Advanced Cervix Cancer

PHOENIX I
Start date: December 2011
Phase: Phase 1
Study type: Interventional

The cervix cancer is the second malignant neoplasia more common between women. The combined treatment involving chemotherapy and radiotherapy was defined as the standard. This study will evaluate the safety, toxicity and maximal tolerated dose (MTD) of everolimus in association with cisplatin and pelvic radiotherapy, in patients with squamous cells carcinoma of uterine cervix, in stages IIB and IIIB.

NCT ID: NCT01217164 Completed - Weight Gain Preterm Clinical Trials

Strategy to Minimize In-hospital Malnutrition in Premature Babies

SPN
Start date: October 2008
Phase: Phase 0
Study type: Interventional

Adequate nutrition is important for preventing malnutrition in the postnatal period and thus optimize growth and development of children born prematurely. To avoid malnutrition is recommended to provide nutrients necessary for a growth rate similar to the intrauterine life. For nearly one decade studying how to minimize in-hospital malnutrition in children born prematurely, especially with gestational age less than 32 weeks or with birth weight below 1,500 g, called newborn very low birth weight (VLBW). Embleton et al.demonstrated that with the current nutritional recommendations (protein between 3.0 and 3.8 g / kg / day), the VLBW had malnutrition caused by protein and calorie cumulative deficit. Poor nutrition in the neonatal period can impair growth and neuromotor and cognitive development after hospital discharge. The investigators hypothesis is that VLBW subjected to aggressive nutrition with protein-calorie high from birth until discharge, would present higher weight gain than the VLBW infants who received routine diet of service, without producing adverse effects.

NCT ID: NCT01215955 Completed - Clinical trials for Diabetes Mellitus, Type 2

Study of Insulin Lispro in Participants With Inadequately Controlled Type 2 Diabetes

AUTONOMY
Start date: December 2010
Phase: Phase 4
Study type: Interventional

Evidence regarding optimal methods of insulin dose adjustment is lacking in the literature. The purpose of this study is to evaluate the efficacy and safety of two approaches to escalate prandial insulin therapy in participants with type 2 diabetes mellitus not achieving adequate glycemic control on basal insulin.

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: 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: 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.