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Cystic Fibrosis clinical trials

View clinical trials related to Cystic Fibrosis.

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NCT ID: NCT02109822 Completed - Cystic Fibrosis Clinical Trials

Pilot Observational Study to Determine Feasibility of a Standardized Treatment of Pulmonary Exacerb. in Patients With CF

STOP-OB-13
Start date: January 2014
Phase: N/A
Study type: Observational

The goal of this research study is to better understand current treatment practices for pulmonary exacerbations (lung infections) and whether the Cystic Fibrosis National Patient Registry (CFFNPR)can be used for this type of study.

NCT ID: NCT02084043 Completed - Asthma Clinical Trials

In Vitro Assessment of a Breath-synchronized Vibrating Mesh Nebulizer During Non Invasive Ventilation

Synchro-Neb
Start date: March 2014
Phase: N/A
Study type: Interventional

Using an adult lung bench model of non invasive ventilation, the aim of the study is to compare an experimental system of breath-synchronized vibrating mesh nebulizer to a conventional vibrating mesh nebulizer during non invasive ventilation in terms of inhaled and lost doses.

NCT ID: NCT02083263 Completed - Cystic Fibrosis Clinical Trials

Non Invasive Ventilation as Airway Clearance in Patients With Cystic Fibrosis

Start date: October 2012
Phase: N/A
Study type: Interventional

With the use of Non invasive ventilation the patients with cystic fibrosis will have better lung function (FEV1).

NCT ID: NCT02070744 Completed - Cystic Fibrosis Clinical Trials

Study to Evaluate Safety and Efficacy of VX-661 in Combination With Ivacaftor in Subjects With Cystic Fibrosis, Homozygous for the F508del-CFTR Mutation With an Open-Label Expansion

Start date: March 2014
Phase: Phase 2
Study type: Interventional

The objective of this study was to evaluate the safety and efficacy of VX-661in combination with ivacaftor in participants with cystic fibrosis (CF) who are homozygous for F508del cystic fibrosis transmembrane conductance regulator (CFTR) mutation

NCT ID: NCT02057458 Completed - Cystic Fibrosis Clinical Trials

Blood Flow and Vascular Function in Cystic Fibrosis

CF-FLOW
Start date: April 2014
Phase: Phase 2
Study type: Interventional

Cystic fibrosis (CF) has many health consequences. A reduction in the ability to perform exercise in patients with CF is related to greater death rates, steeper decline in lung function, and more frequent lung infections. However, the physiological mechanisms for this reduced exercise capacity are unknown. The investigators laboratory recently published the first evidence of systemic vascular dysfunction in patients with CF. Therefore, it is reasonable to suspect that the blood vessels are involved with exercise intolerance in CF. This study will look at how 1) blood flow and 2) artery function contribute to exercise capacity in CF.

NCT ID: NCT02056132 Completed - Cystic Fibrosis Clinical Trials

Breath Condensate Study in Patients With Cystic Fibrosis.

Start date: February 2014
Phase:
Study type: Observational

There is an urgent need for a noninvasive method to diagnose bronchial infections and exacerbations in patients with Cystic Fibrosis (CF). The current method to diagnosed infections involves either collecting a sputum sample or obtaining a bronchoalveolar lavage (BAL). However, some patients cannot produce sputum. At the same time the decision of when a patient has an exacerbation continues to be very subjective. In this exploratory study, we propose a new, noninvasive method to diagnose bronchial infections and to evaluate possible markers of inflammation that can assist in a noninvasive way in the determination of exacerbations.

NCT ID: NCT02054377 Completed - Cystic Fibrosis Clinical Trials

Cystic Fibrosis- Children and Adults Tai Chi Study

CFCATS2
Start date: June 2014
Phase: N/A
Study type: Interventional

Cystic fibrosis (CF) is a progressive disease. Symptoms include coughing, poor lung ventilation, recurrent infections, poor weight gain, diarrhoea, malnutrition, stress, frustration, depression, irritability, worry, insomnia, behavioural issues and missed school/work. Tai chi, a Chinese form of exercise, uses slow choreographed movements, breathing exercises and mindfulness. Research suggests tai chi can improve physical and emotional wellbeing for various chronic conditions. This study compares methods of teaching tai chi to 70 people with CF, and evaluates the effect on symptoms and quality of life. Adults and children with CF will be recruited and randomly allocated to an intervention group or a control group. The former will receive 8 individual face to face sessions of tai chi over a 3 month period and a video and handouts to aid home practice. The latter will have routine care for the first 12 weeks, followed by 8 individual online sessions of tai chi over a 3 month period, and a video and handouts for home practice. Both groups will be encouraged to practice tai chi at home in the months following the taught sessions. Questionnaire data on how participants and their carers are coping with CF, any general improvements in wellbeing, and differences in other clinical outcomes (medication etc.)will be collected. Data will be collected at the beginning and end of the intervention, and at 6 and 9 months post intervention and differences between the 2 groups compared over time. Feedback from on line focus groups will ask about their experiences, feasibility of learning and practicing of tai chi, engagement with the process, perceived health impact, and experiences of participation. It is hoped that the study may show how Tai Chi can help people with CF to maintain their health through mindful exercise, and improve troublesome symptoms like sleep and anxiety.

NCT ID: NCT02054156 Completed - Cystic Fibrosis Clinical Trials

OPTIMIZing Treatment for Early Pseudomonas Aeruginosa Infection in Cystic Fibrosis

OPTIMIZE
Start date: June 2014
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to compare the effects of treatment with tobramycin solution for inhalation (TIS) with and without azithromycin in people with cystic fibrosis (CF) age 6 months to 18 years who have early isolation of Pseudomonas aeruginosa (Pa) from a respiratory culture. Specimens of blood and sputum or throat swabs will be taken during the study along with pulmonary function testing. Participants will receive initial treatment with TIS followed additional treatment with TIS if quarterly respiratory cultures are positive for Pa in addition to either azithromycin or placebo for 18 months.

NCT ID: NCT02043717 Completed - Cystic Fibrosis Clinical Trials

Increased Vitamin D Reduces Pulmonary Exacerbations in CF

Start date: January 2014
Phase: N/A
Study type: Observational [Patient Registry]

The investigators study is designed to test the hypothesis that correction of vitamin D in CF patients can increase their lung function and decrease the number of their pulmonary exacerbations.

NCT ID: NCT02039986 Completed - Cystic Fibrosis Clinical Trials

Ivacaftor (Kalydeco) and Insulin in Cystic Fibrosis (CF)

Start date: January 6, 2014
Phase:
Study type: Observational

This study is aimed at better understanding the impact of ivacaftor upon insulin and incretin secretion and glucose tolerance in patients with Cystic Fibrosis with a glycine (G551D) mutation. Investigators hypothesize that treatment with ivacaftor improves insulin secretion in individuals with CF.