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Cystic Fibrosis clinical trials

View clinical trials related to Cystic Fibrosis.

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NCT ID: NCT00056147 Completed - Cystic Fibrosis Clinical Trials

Study of INS37217 Inhalation Solution in Mild to Moderate Cystic Fibrosis Lung Disease

Start date: April 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and effectiveness of multiple dosages of INS37217 compared to placebo over 28 days in subjects with mild to moderate cystic fibrosis (CF) lung disease. Study drug will be administered through a nebulizer (a device that delivers medication as a mist by breathing it in).

NCT ID: NCT00043342 Completed - Cystic Fibrosis Clinical Trials

Study of Interferon Gamma-1b by Injection for the Treatment of Patients With Cystic Fibrosis

Start date: April 2002
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this research study is to evaluate the safety, tolerability, and efficacy of Interferon gamma-1b (IFN-gamma 1b) when administered by subcutaneous injection over a period of 4 weeks to patients with mild-to-moderate cystic fibrosis. Additionally, preliminary assessments on the effects of IFN-gamma 1b on lung function and other indicators of health will be made.

NCT ID: NCT00043316 Completed - Cystic Fibrosis Clinical Trials

Interferon Gamma-1b by Inhalation for the Treatment of Patients With Cystic Fibrosis

Start date: February 2001
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this research study is to evaluate the safety and effectiveness of Interferon gamma-1b (IFN-g 1b) on lung function when given to patients with cystic fibrosis by inhalation (breathed into the lungs) three times a week for 12 weeks. The FDA has not approved Interferon gamma-1b for use with cystic fibrosis patients, which is the condition being examined in this study.

NCT ID: NCT00043225 Completed - Cystic Fibrosis Clinical Trials

The Role of Bacteria and Genetic Variations in Cystic Fibrosis

Start date: June 20, 2001
Phase:
Study type: Observational

This study will examine 1) the role of hereditary factors in cystic fibrosis; i.e., the relationship of the disease to specific gene variations, and 2) the role of bacterial products involved in lung infections substances produced by bacteria may worsen the disease. Patients with cystic fibrosis who are being followed by the Medical College of Wisconsin or the University of Wisconsin-Madison are eligible for this study. Participants will have blood tests, pulmonary function tests, a sputum culture, and buccal swabbing (cotton swabbing of the inside of the cheek to collect cells for DNA study). In addition, their medical records will be reviewed for a history of lung infections and the results of various tests, including pulmonary function studies, chest X-rays and bacterial cultures. Blood samples collected previously at the Medical College of Wisconsin or the University of Wisconsin-Madison will also be analyzed for antibodies to bacteria. Although this is a one-time study, participants may be asked to return for repeated tests. ...

NCT ID: NCT00037778 Completed - Cystic Fibrosis Clinical Trials

Genetic Modifiers of Cystic Fibrosis: Sibling Study

Start date: September 2001
Phase: N/A
Study type: Observational

The purpose of this study is to identify modifier genes in cystic fibrosis (CF).

NCT ID: NCT00034515 Completed - Cystic Fibrosis Clinical Trials

A Study in Adult and Pediatric Patients With Cystic Fibrosis

Start date: June 2001
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this ascending dose group study is to assess the safety, tolerability, and effects of multiple dose levels of INS37217 and placebo followed by five days twice daily treatment with maximum tolerated dose administered by inhalation via the Pari LC Star nebulizer in adult and pediatric patients with cystic fibrosis

NCT ID: NCT00027183 Completed - Cystic Fibrosis Clinical Trials

Role of Toxins in Lung Infections Caused by Pseudomonas Aeruginosa

Start date: March 17, 1998
Phase:
Study type: Observational

Some bacteria that cause disease can produce toxic substances that may worsen the disease. Pseudomonas aeruginosa is a bacteria that can produce a variety of toxins and is of special interest for patients with cystic fibrosis and repeated long term lung infections. The goal of this study is to determine whether specific toxins produced by Pseudomonas aeruginosa may be important in the disease process of chronic lung infections of patients with cystic fibrosis. This study will attempt to measure bacterial production of toxins in blood and sputum and immune system response to toxins in the blood....

NCT ID: NCT00016744 Completed - Cystic Fibrosis Clinical Trials

Phenylbutyrate/Genistein Duotherapy in Delta F508-Homozygous(for Cystic Fibrosis)

Start date: September 2001
Phase: Phase 1/Phase 2
Study type: Interventional

We are testing a new combination of medicines, to determine if they could be used to treat cystic fibrosis (CF). Subjects with CF who have two copies of the most common mutation (change) found in patients with CF called DF508. CF is caused by a lack of chloride movement in the nose, sinuses, lungs, intestines, pancreas and sweat glands. We are conducting this study to determine the safety of using a combination of two medicines, Phenylbutyrate and Genistein, to improve the ability of the cells lining the nose to regulate movement of salt (chloride) and water in people with CF. Phenylbutyrate has been extensively used to treat patients with rare metabolic diseases (which are very different from CF), Phenylbutyrate is an investigational drug for the purpose of this study. Genistein is a naturally occurring substance that is found in food products such as soy and tofu, but is also an investigational drug for this study. Both drugs may be able to restore normal chloride movements in body organs and glands. We will be studying salt and water in the nose movement by a technique called nasal transepithelial potential difference (NPD).

NCT ID: NCT00016445 Completed - Cystic Fibrosis Clinical Trials

Phase II Study of Growth Hormone in Children With Cystic Fibrosis

Start date: February 2001
Phase: Phase 2
Study type: Interventional

OBJECTIVES: I. Determine the effect of growth hormone on height, height velocity, body weight, and lean body mass in patients with cystic fibrosis. II. Determine the effect of growth hormone on pulmonary function in these patients. III. Determine the impact of this drug on the quality of life in these patients. IV. Determine if the clinical response from this drug is sustained in these patients.

NCT ID: NCT00015756 Completed - Cystic Fibrosis Clinical Trials

Tissue Collection From People With Cystic Fibrosis

Start date: May 2, 2001
Phase: N/A
Study type: Observational

This study will examine the relationship between bacterial products in lung infections in cystic fibrosis and disease severity. It will examine plasma and lung tissue from cystic fibrosis patients. Patients with cystic fibrosis and having certain genetic characteristics, who are between 9 and 65 years of age and any cystic fibrosis patient undergoing lung transplantation at INOVA Fairfax Hospital in Fairfax, Virginia, may be eligible for this study. Patients who cannot undergo apheresis may be asked to provide up to an additional 100 cc (7 tablespoons) of blood for research to look at bacterial products. Lung specimens of participating transplant patients will be collected at INOVA Fairfax Hospital. Patients who participate in the apheresis portion of the study will be admitted to the NIH Clinical Center for 2 to 3 days. Apheresis is a procedure for collecting large quantities of specific blood components. For this study, plasma-the liquid part of the blood-will be collected. For the procedure, whole blood is collected through a needle in an arm vein, similar to donating blood. The blood is separated into its components by centrifugation (spinning), the plasma and white cells are extracted and collected in a bag, and the red cells are returned to the body, either through the same needle or through another needle in the other arm. During the hospital stay, patients may also be asked to participate in other cystic fibrosis studies involving blood tests, an echocardiogram (ultrasound test of the heart), urine pregnancy test, and pulmonary function (breathing) tests.