Cystic Fibrosis

Join Clinical Trials for Cystic Fibrosis

Join Clinical Trials for Cystic Fibrosis

General Purpose: Individuals who develop cystic fibrosis do so because they have inherited two faulty genes, one from each parent. As such, cystic fibrosis is caused solely by genetic mutations and is most common among Caucasians of northern European ancestry.

However, it is also common among Latinos as well as certain groups of American Indians. Because the underlying cause of cystic fibrosis is known, much research continues to focus on the role that genes play in the development of the lung disease associated with cystic fibrosis.

In addition, there is considerable research investigating new and improved treatment options for lung infections in children with cystic fibrosis, as well as studies that are seeking to determine how new medicines and other therapies can help to improve the quality of life for people with this burdensome condition.

Continued … Cystic Fibrosis Clinical Trials (Click to Open)

Join Clinical Trials for Cystic Fibrosis

Cystic Fibrosis Clinical Trials

What Will Clinical Trials for Cystic Fibrosis Be Like?

When participating in Clinical Trials for Cystic Fibrosis, a few common tests and procedures may be involved; however, the ultimate design of the particular study will determine which specific procedures you will undergo.

Many studies will involve the use of blood tests to screen for genetic characteristics.  A chest x-ray may also be used to view the heart, lungs, and blood vessels in order to observe inflammation, scarring, and air-trapping. In addition, some studies may involve the use of a sinus x-ray in order to determine the presence of sinusitis, which is a common complication of cystic fibrosis.

Additional tests and procedures that may also be involved in cystic fibrosis research include: lung function tests; sputum/spit cultures; prenatal screening (for pregnant women); and simple blood testing to determine if non-symptomatic individuals are carriers for the genetic mutations that cause cystic fibrosis. Genetic counseling may also be involved in some clinical trials.

Typical Cystic Fibrosis Clinical Trial Protocol:

Research related to cystic fibrosis covers a wide range of topics. Specific examples might Cystic Fibrosis Clinical Trialsinclude the following types of studies:

  • A study designed to investigate how genetic mutations actually lead to the symptoms of cystic fibrosis.
  • A study designed to investigate newly-developed respiratory therapies, antibiotics, anti-viral medications, and other treatments for lung infections in children with cystic fibrosis.
  • A study designed to investigate the association between smoking status and genetic mutations that lead to the development of cystic fibrosis.
  • Studies evaluating the feasibility and effectiveness of various types of exercise on the symptoms associated with cystic fibrosis.
  • A study designed to evaluate how existing treatments and newly-developed treatments compare in their ability to improve the quality of life among patients with cystic fibrosis.

Suggested Search Terms:

“cystic fibrosis exacerbation,” “cystic fibrosis therapy,” “cystic fibrosis gene therapy,” “cystic fibrosis children,” “cystic fibrosis exercise,” and “cystic fibrosis smoking.” 

Current Search Term:

“Cystic Fibrosis”


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