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Chronic Disease clinical trials

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NCT ID: NCT00358358 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Chronic Obstructive Pulmonary Disease Endpoints Study

Start date: March 2006
Phase: Phase 4
Study type: Interventional

This study will last for approximately 14 weeks and will involve 5 visits. The study is being carried out to look at different ways of measuring the effect of drug treatment on COPD. COPD is a respiratory disease which can affect your breathing and daily life. Symptoms of COPD can include breathlessness, cough, and wheeze. COPD varies enormously from patient to patient. The effects of drug treatment are usually measured by conducting lung function tests (breathing tests) using a machine called a spirometer but this does not always provide a complete picture of how well your COPD is responding. In this study we therefore want to look at new and more sensitive ways of measuring COPD. The results of this research will help in the assessment of new drugs for COPD in the future.

NCT ID: NCT00355342 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Bone Mineral Density Study In Patients With Chronic Obstructive Pulmonary Disease. DISKUS® Inhaler is a Trademark of the GSK Group of Companies.

Start date: April 28, 2004
Phase: Phase 4
Study type: Interventional

This study will last up to 3 years. You will visit the clinic up to 14 times. Certain visits will include lung function tests and scans of your bones. The purpose of this study is to determine the effect of the steroid component of an inhaled product on bone mineral density in patients with Chronic Obstructive Pulmonary Disease (COPD).

NCT ID: NCT00354666 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Single Doses GSK159797 On Patient Safety And Lung Function In Patients With Mild To Moderate Asthma

Start date: September 2004
Phase: Phase 2
Study type: Interventional

This study was designed to test safety aspects and effects on lung function of a new dry powder version of GSK159797 for asthmatic subjects to inhale. This will allow comparison with previous studies which have only used inhalation of the drug as a vapour.

NCT ID: NCT00351676 Completed - Clinical trials for Diabetes Mellitus, Type 2

Capturing Outcomes of Clinical Activities Performed by a Rounding Pharmacist Practising in a Team Environment

Start date: February 2006
Phase: Phase 4
Study type: Interventional

We, the researchers, propose to link a clinical pharmacist with an internal medicine or family medicine team to provide pharmaceutical care to all patients assigned to the team. The hypothesis is that through this team based approach, pharmacists will act as a resource for providing pharmacotherapeutic advice during the drug therapy decision making process and promote optimal drug use by identifying and resolving actual and potential drug related problems. This study is designed to test this hypothesis, by assessing the impact of this intervention on evidence based, quality of drug therapy indicators, for patients admitted with heart failure (HF), chronic obstructive pulmonary disease (COPD), community acquired pneumonia (CAP), type 2 diabetes mellitus (T2DM), and stable coronary artery disease (CAD).

NCT ID: NCT00347139 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Repeat Doses Of A New Medication (GW642444) In Asthmatic Patients

Start date: May 23, 2006
Phase: Phase 2
Study type: Interventional

In order to obtain information on a wider range of doses of GW642444 (a possible new medication to treat asthma) than has been previously examined in asthmatic patients, this current study will be conducted at doses of 25 100 and 400 mcg of GW642444 and will be compared with salmeterol (50 mcg twice daily). This study will be conducted in a similar manner to a study that has already been completed (study number B2C101762) which examined repeat doses of 50, 100 and 200 mcg of GW642444. The data obtained will compliment the data from study B2C101762 and will provide confidence (or not) that the desired bronchodilation can be achieved and maintained without undesirable side effects.

NCT ID: NCT00345137 Completed - Glomerulonephritis Clinical Trials

Effects of Systemic NO-Inhibition on Renal Hemodynamics in Patiens With Polycystic Kidney Disease and Chronic Glomerulonephritis

Start date: n/a
Phase: Phase 1
Study type: Interventional

The study tests the hypothesis that systemic and renal nitric oxide availability is changed in polycystic kidney disease and chronic glomerulonephritis.

NCT ID: NCT00341536 Completed - Chronic Diseases Clinical Trials

Feasibility Study for Prospective Diet and Lifestyle Cohorts in Delhi, Kerala, and Kolkota, India

Start date: June 17, 2004
Phase:
Study type: Observational

This pilot study will examine the potential for health, diet and lifestyle research in Delhi, Kerala, and Kolkota, India. It will: 1) evaluate the adequacy of the existing infrastructure for a large-scale epidemiologic investigation and follow-up; 2) obtain a characterization of the Indian diet; 3) determine study end-points; 4) evaluate the feasibility of collecting and analyzing biologic samples within India; and 5) evaluate the ability of centers to recruit subjects and collect data. Indian men and women between 35 and 70 years of age who have resided in the study area (Delhi, Kerala, or Kolkota) for at least 1 year may be eligible for this study. Participants will undergo the following tests and procedures: Part A: Diet and Lifestyle (2 visits) - Questionnaires on medical history and treatment practices, including questions on reproductive history - Brief medical examination - Body measurements, including height, weight, forearm circumference, thighs, hips, stomach, skin thickness of the back and triceps (back of the arms) - Blood draw for research, including studies of gene changes that affect the way the body uses nutrients - Collection of toenail clippings for research tests - Interview about: 1) dietary habits and understanding of the relationship of diet to health; 2) lifestyle, work, and family health; and 3) moving history (how often subject has moved in the past 5 years, addresses of past homes, and plans for future moves) Part B: Understanding Diet (6 visits) - Interview at each visit about food and drink consumed the day before the interview - 2 blood draws - 24-hour urine collection - Physical activity monitor. The subject wears a small device placed on the belt or waist of the pants for a specified time to measure the amount of movement performed. Part C: Medical Follow-up Patterns (1 visit) -Answer questions about medical history, treatment practices, and dietary habits

NCT ID: NCT00333710 Completed - Hepatitis C Clinical Trials

Evaluating a Telehealth Treatment for Veterans With Hepatitis C and PTSD

Start date: September 2006
Phase: N/A
Study type: Interventional

The main objective of this proposal is to develop and test the efficacy of two interventions (a telehealth and face-to-face intervention) designed to improve quality of life, self-care, motivation to engage in healthcare, and psychological distress in patients diagnosed with HCV and PTSD. It is hypothesized that

NCT ID: NCT00328848 Completed - Hypertension Clinical Trials

After Discharge Management of Low Income Frail Elderly

Start date: October 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether comprehensive post-hospitalization interdisciplinary care management can be an effective care delivery model to improve outcomes in low-income frail elderly.

NCT ID: NCT00328484 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Comparison of Two Programs to Encourage Physical Activity in Individuals With Chronic Obstructive Pulmonary Disease

Start date: January 2002
Phase: Phase 3
Study type: Interventional

Chronic obstructive pulmonary disease (COPD) is a chronic lung disease. Symptoms include shortness of breath, wheezing, and difficulty exercising. Increasing exercise and physical activity may relieve the symptoms of COPD and may also slow the progression of the disease. The purpose of this study is to evaluate the effectiveness of a lifestyle activity program versus a traditional exercise program at increasing the amount of physical activity among individuals with COPD.