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Chronic Disease clinical trials

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NCT ID: NCT00105911 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

A Cognitive-Behavioral Intervention for Depression and Anxiety in COPD

Start date: July 2002
Phase: N/A
Study type: Interventional

The literature and our preliminary studies found that in COPD patients, psychosocial factors affect quality of life (QOL) and functioning more than would be expected given the severity of their disease. To improve QOL and functioning in the approximately 50% of COPD patients with significant anxiety and/or depressive symptoms, interventions are needed. Much research documents the utility of cognitive behavioral therapy (CBT) in treating depression and anxiety, showing it to have promise as a self-management intervention to improve QOL in COPD patients.

NCT ID: NCT00104637 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Sildenafil for Chronic Obstructive Pulmonary Disease

Start date: February 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if sildenafil improves the exercise capacity and lung function of patients with chronic obstructive pulmonary disease.

NCT ID: NCT00103922 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Study In Subjects With COPD (Chronic Obstructive Pulmonary Disease)

Start date: November 2004
Phase: Phase 3
Study type: Interventional

This study was designed to determine if the investigational drug is effective and safe in individuals with COPD (chronic pulmonary disease)

NCT ID: NCT00097773 Completed - Cystic Fibrosis Clinical Trials

Comparison of Two Treatment Regimens to Reduce PA Infection in Children With Cystic Fibrosis

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

Cystic fibrosis (CF) is a chronic disease that significantly affects an individual's lung function. Antibiotic medications have been proven effective at reducing Pseudomonas aeruginosa (PA) infection, which is one of the main causes of death in individuals with CF. The purpose of this study is to compare the effectiveness of treatment based on quarterly culture results versus consistent quarterly antibiotic treatment at reducing PA infection in children with CF.

NCT ID: NCT00096811 No longer available - Hepatitis B Clinical Trials

Entecavir for Subjects With Chronic Hepatitis B Infection: An Early Access Program

Start date: September 2003
Phase: N/A
Study type: Expanded Access

The purpose of this clinical research study is to provide entecavir to subjects with chronic Hepatitis B infection who have failed or who have demonstrated intolerance of marketed therapies or for those in whom use of these agents is contraindicated and that have no other available treatment options.

NCT ID: NCT00096785 Completed - Hepatitis B Clinical Trials

Comparative Trial of Entecavir Versus Adefovir in the Treatment of Chronic Hepatitis B Infection

Start date: December 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate antiviral activity and efficacy of entecavir (ETV) compared to adefovir in adults with chronic hepatitis B who have not been treated yet with an antiviral medicine.

NCT ID: NCT00051792 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Yoga for Treating Shortness of Breath in Chronic Obstructive Pulmonary Disease (COPD)

Start date: January 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of yoga in reducing shortness of breath in people with chronic obstructive pulmonary disease (COPD). Patients in this study must have moderate to severe COPD and be primarily limited by shortness of breath.

NCT ID: NCT00038649 Terminated - Clinical trials for Myelogenous Leukemia, Chronic, Chronic Phase

Therapy of Early Chronic Phase CML With Higher-Dose Gleevec, Alpha Interferon, and Low-Dose Ara-C

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

The goal of this clinical research study is to see if higher doses of imatinib mesylate (Gleevec, STI571) can improve chronic myelogenous leukemia (CML) in chronic phase.

NCT ID: NCT00038597 Completed - Clinical trials for Myelogenous Leukemia, Chronic

Phase II Study of SCH66336, A Farnesyltransferase Inhibitor in Chronic Myelogenous Leukemia (CML)

Start date: April 30, 2001
Phase: Phase 2
Study type: Interventional

The goal of this research is to see if giving the drug SCH66336 by mouth can improve the disease in patients with chronic or accelerated phase CML. The safety of this treatment will also be studied.

NCT ID: NCT00037973 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Effect of Ventilation-Feedback Training on Exercise Performance in COPD

Start date: August 2000
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to determine whether individuals with Chronic Obstructive Pulmonary Disease (COPD) who complete ventilation-feedback training combined with a moderately-high intensity exercise and upper body strength program will demonstrate significantly longer exercise duration on a constant work rate treadmill test when compared to subjects who are randomly assigned to a moderately-high intensity exercise and upper body strength training program without ventilation-feedback or ventilation-feedback only. Secondary study objectives are to determine whether individuals with COPD who complete ventilation-feedback training combined with a moderately-high intensity exercise and upper body strength training program will demonstrate significantly: (a) greater exercise tolerance and aerobic power; (b) lower perception of breathlessness during progressive and constant work rate leg-cycle and treadmill exercise testing; (c) higher tidal volume and lower breathing frequency during constant work rate and at any given workload during progressive testing; (d) lower score on the Chronic Respiratory Disease Questionnaire indicating improved quality of life; (e) higher transition focal score (less dyspnea) on the Transition Dyspnea Index; (f) maintain a sustained breathing-pattern adjustment to exercise when compared to subjects who are randomly assigned to a moderately-high intensity exercise and upper body strength program without ventilation-feedback or ventilation-feedback only.