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NCT ID: NCT00651989 Not yet recruiting - Clinical trials for Normal Foveal Thickness

Agreement Between Spectral Domain and Time Domain Optical Coherence Tomography (OCT)

Start date: April 2008
Phase: N/A
Study type: Observational

Optical coherence tomography (OCT) is a well-established and safe technique that offers the possibility of visualizing retinal structure and measuring retinal thickness. Time-domain (TD)OCT is considered the "gold standard" technique for retinal thickness measurements. Spectral-domain (SD) OCT has to face the gold standard technique prior to obtain scientific and clinical consensus. In our study in healthy subjects foveal thickness will be measured with both TD and SD OCT , and the data will be compared to evidence any difference between the two retinal measurements techniques.

NCT ID: NCT00658151 Not yet recruiting - Clinical trials for Antibiotic-Associated Diarrhea

Ultrasound Diagnosis of Antibiotic Associated Diarrhea

Start date: April 2008
Phase: N/A
Study type: Observational

The hypothesis is that there are unique sonographic characteristics of antibiotic-associated diarrhea. We will compare the ultrasound findings in patients who received antibiotics and developed diarrhea to toxin analysis for clostridium difficile in stool in order to find differences in the sonographic findings in the positive and negative cases.

NCT ID: NCT00659854 Not yet recruiting - Clinical trials for Obstructive Sleep Apnea Syndrome

Cow's Milk Allergy in Infants With Obstructive Sleep Apnea (OSA)

Start date: April 2008
Phase: N/A
Study type: Interventional

Cow's milk allergy may be involved in the evolution of sleep apnea in infants. The study will assess the effects of specifies diet changes (i.e. non-milk based formula) on the infant. Specifically , infants will be investigated by sleep studies in order to test this hypothesis.

NCT ID: NCT00661063 Not yet recruiting - Pain Clinical Trials

Diabetic Neuropathy Topical Treatment

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

Comparative study of efficacy and safety of ketamine, clonidine, mixture of both and placebo in patients with diabetic neuropathic pain

NCT ID: NCT00667706 Not yet recruiting - Morbid Obesity Clinical Trials

Laparoscopic Roux-en-Y Gastric Bypass Versus Laparoscopic Sleeve Gastrectomy

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

The sleeve gastrectomy that has been utilized as a first-stage bariatric procedure to reduce surgical risk in high-risk patients by induction of weight loss is now gaining popularity as a standalone procedure for the treatment of morbid obesity. It appears to be a technically easier and/or faster laparoscopic procedure than Roux-en-Y gastric bypass. It brings good weight loss results, in some studies even comparable to the RYGB and Biliopancreatic Diversion with Duodenal Switch. The mechanism of action is assumed to be purely restrictive, but some neurohumoral interaction may exist. Almost no data exist on the influence of the sleeve gastrectomy on the medical and general quality of life or resolution of comorbidities. The rates of the comorbidities resolution 12 to 24 months after sleeve gastrectomy has been reported in the range that seems to be higher than for the purely restrictive procedures. Our goal is to to compare the surgical and weight loss outcomes between the two procedures, their influence on resolution of common comorbidities and on quality of life change. 150 eligible candidates will be randomized into two groups, one will undergo Laparoscopic Sleeve Gastrectomy, the other will have Laparoscopic Roux-en-Y Gastric Bypass done. Detailed evaluation and preoperative questionnaires will be used to obtain demographic and medical data, and quality of life will be assessed. General metabolic and nutritional work up will be done, and will be reassessed at different intervals up to 5 years, in order to compare the short and long term results of the two procedures.

NCT ID: NCT00365521 Not yet recruiting - Organ Transplants Clinical Trials

Prophylactic Photodynamic Therapy to Organ Transplant Patients

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

To evaluate a possible prophylactic efficacy of photodynamic therapy on the incidence of non-melanoma skin cancer, actinic keratoses, warts and keratoses in recently organ transplanted recipients.

NCT ID: NCT00431743 Not yet recruiting - Breast Surgery Clinical Trials

Fluid Infusion During Breast Surgery

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

The investigators want to investigate the effects of two different kinds of fluid infusions given during varicose vein surgery. Both types of fluid are regularly given during surgery, and the investigators want to compare their respective effects on balance, nausea/vomiting and orthostatic function after surgery. The investigators' hypothesis is that using a colloid solution will improve orthostatic function, balance, nausea/vomiting and reduce hospital stay.

NCT ID: NCT00612287 Not yet recruiting - Chronic Pain Clinical Trials

Sublingual Buprenorphine for Chronic Pain

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

The purpose of this study is to develop and pilot test clinical guidelines for the use of buprenorphine for the treatment chronic pain among patients with substance abuse histories. Buprenorphine, an opioid medication, holds promise as a treatment of chronic pain because, compared to most other opioid analgesics, it has a high safety profile, a low level of physical dependence, and mild withdrawal symptoms on cessation. Moreover there are promising reports from Europe of its use as a skin patch to treat chronic pain as well as clinical reports in the U.S. that it may be effective when used sublingually (placed under the tongue). This study will test the sublingual formulation.

NCT ID: NCT00719485 Not yet recruiting - Clinical trials for Decompression, Surgical

A Study on the Use of Educational Programs Prior to Lumbar Spinal Surgery

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

This study evaluated the hypothesis that the implementation of an educational program that informs spine patients about their condition, treatment options, prioritization on the wait list, and post-operative care would improve functional outcome and quality of life scores following surgery

NCT ID: NCT00763308 Not yet recruiting - Clinical trials for Cardiovascular Diseases

A Web-Based Cardiovascular Intervention for the Workplace

Start date: April 2009
Phase: Phase 1
Study type: Interventional

Heart disease is the leading cause of death in the United States, accounting for approximately 700,000 deaths a year. Heart disease can take many forms, including heart attacks, coronary artery disease, aneurysms, high blood pressure, and strokes. However, people can change things in their life to reduce the risk of getting heart disease. This study will first create an Internet-based program to help teach people about reducing heart disease risk and will then test the program in a workplace setting.