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NCT ID: NCT00497666 Not yet recruiting - Diabetes Clinical Trials

Association Between Rosiglitazone Use and Clinical Course of Diabetic Nephropathy: Population-Based Study

Start date: August 2007
Phase: N/A
Study type: Observational

Recent data show that Rosiglitazone treatment can reduce proteinuria in diabetic patients. However, currently there are no trials that examine the effects of Rosiglitazone on kidney disease progression, that is, doubling of serum creatinine or time to onset of end-stage renal disease, in patients with diabetic nephropathy. We decided to study retrospectively the possible association between rosiglitazone use and clinical course of diabetic nephropathy, including rate of deterioration of renal function, appearance and progression of microalbuminuria/proteinuria, survival and acceptance to renal replacement therapy.

NCT ID: NCT00497042 Not yet recruiting - Clinical trials for Teeth, Endodontically-Treated

Safety and Efficacy of Using the Endodontic Self Adjusting File - SAF for Root Canal Treatment

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

The study’s primary goal is to assess the safety of the SAF (Self Adjusting File) device for root canal treatments. The study’s secondary goal is to evaluate the effectiveness of the SAF device for root canal treatments

NCT ID: NCT00496938 Completed - Clinical trials for Coronary Artery Disease

XIENCE V: SPIRIT WOMEN

Start date: July 2007
Phase: Phase 4
Study type: Interventional

The purpose of this Clinical Evaluation is the continued assessment of the XIENCE Everolimus Eluting Coronary Stent System (XIENCE V® and XIENCE PRIME™ EECSS) with the primary focus on clinical outcomes in the treatment of female patients with de novo coronary artery lesions, and the characterization of the female population undergoing stent implantation with a XIENCE stent.

NCT ID: NCT00496925 Completed - Clinical trials for Obsessive Compulsive Disorder

Examining the Usage of Dopamine Blockers in OCD Patients

Start date: November 2007
Phase: N/A
Study type: Observational

We examine the usage of Dopamine blockers in OCD patients. We want to examine their frequency of usage, compare the course of the disease between those who receive and those who do not receive Dopamine blockers, and efficacy of the treatment. The study will be done in two stages: 1. Collecting information the usage of Dopamine blockers from 150 OCD patients' files. 2. interviewing 60-70 patients to see the difference those who receive and those who do not receive Dopamine blockers in their current severity of disease.

NCT ID: NCT00496899 Terminated - Labor Clinical Trials

Clinical Evaluation of New Computerized Labor Monitoring System

CLM
Start date: June 2007
Phase: N/A
Study type: Observational

The study is an open label feasibility study. The purpose of the study is to evaluate the ease of use of the Cervical ITR in terms of duration of attachment and number of detachments.

NCT ID: NCT00496769 Completed - Atrial Fibrillation Clinical Trials

A Phase III Study of Apixaban in Patients With Atrial Fibrillation

AVERROES
Start date: August 31, 2007
Phase: Phase 3
Study type: Interventional

The purpose of this clinical research study is to determine whether apixaban is more effective than acetylsalicylic acid in the prevention of strokes associated with patients with atrial fibrillation. The safety of this treatment will also be studied.

NCT ID: NCT00496288 Recruiting - Breast Cancer Clinical Trials

Prophylactic Irradiation to the Contralateral Breast for BRCA Mutation Carriers Undergoing Treatment for Breast Cancer

Start date: March 2008
Phase: Phase 2
Study type: Interventional

Women with BRCA germline mutations face a very high risk of developing breast cancer during their lives. It was shown that for carrier patients, breast conservation, comprising of lumpectomy followed by whole breast radiation, was not associated with increased risk of ipsilateral breast cancer recurrence as compared with non carriers (10-15% over 10 years), especially if they also underwent prophylactic oophorectomy. Yet their risk of subsequent contralateral breast cancer was significantly increased, reported as high as 25-30% over 10 years and 40% over 15 years, as compared to 3% and 7% respectively in non carriers. The reduction in ipsilateral disease was attributed to radiation of the affected breast. We propose that for breast cancer patients with BRCA germline mutation that choose to have breast-conserving therapy and refuse prophylactic contralateral mastectomy, prophylactic radiation to the contralateral breast may reduce the rate of subsequent contralateral breast cancer and offer an option for risk reduction.

NCT ID: NCT00496184 Completed - Vulvodynia Clinical Trials

Efficacy Study of Topical Application of Nifedipine Cream to Treat Vulvar Vestibulitis

Start date: April 2006
Phase: Phase 3
Study type: Interventional

To evaluate the use of topical application of Nifedipine cream for the treatment of Provoked localized Vulvodynia (vestibulitis, vestibulodynia).

NCT ID: NCT00495443 Not yet recruiting - Hirsutism Clinical Trials

Enhanced Safety Aesthetic Laser System

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

The purpose of this study is to determine whether a new laser system provides better safety and efficacy than existing lasers in popular cosmetic procedures such as hair removal, treatment of cosmetically disturbing vascular lesions and rhytides.

NCT ID: NCT00495430 Active, not recruiting - Healthy Clinical Trials

Vibration Response Imaging in Healthy Subjects

Start date: December 2004
Phase: N/A
Study type: Observational

The primary purpose is to test intersubject variability and establish the qualitative features of normal VRI images and the range of normality of the VRI quantitative lung data values that may be used to differentiate normal from abnormal breath sound distribution. Our hypothesis was that VRI breath sound images of healthy subjects are similar in a qualitative and quantitative manner.