Asthma Clinical Trial
Official title:
A Study to Identify a Transcriptomic Profile Indicative of Cycle AMP Pathway Activation in the Lung
| NCT number | NCT00331292 |
| Other study ID # | CRB100706 |
| Secondary ID | |
| Status | Terminated |
| Phase | N/A |
| First received | May 26, 2006 |
| Last updated | October 15, 2008 |
| Start date | August 2006 |
| Verified date | October 2008 |
| Source | GlaxoSmithKline |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Food and Drug Administration |
| Study type | Observational |
The primary goal of this study is to identify a gene or panel of genes which are differentially expressed in lung cells and tissue from asthmatic patients following administration of Ipratropium bromide and eiTher nebulised Albuterol or saline. Each subject in this study will undergo two bronchoscopies.
| Status | Terminated |
| Enrollment | 30 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 45 Years |
| Eligibility |
Inclusion criteria: - Have a history of intermittant asthma. - Have asthma symptoms less than once per week. - Have no other significant disease. - Do not take regular oral or inhaled steroids. - Are a non-smoker for the past 12 months with a pack history of less than 5 years. Exclusion criteria: - Have a history of drug or alcohol abuse. - Have poorly controlled asthma or a history of life-threatening asthma. - Have a history of hypersensitivity to bronchodilators. - Are unable to abstain from inhaled steroids from 14 days prior to the first study visit until completion of the study. - Have received oral steroids within 3 months of study entry. - Have been hospitalized for your asthma within 3 months of study entry. - Have had treatment with an investigational drug within 30 days or 5 half-lives (whichever is longer) preceding the first dose of study medication. |
Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| United States | GSK Investigational Site | Philadelphia | Pennsylvania |
| Lead Sponsor | Collaborator |
|---|---|
| GlaxoSmithKline |
United States,
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