Prevalence of Alpha-1 Antitrypsin Deficiency in Chronic Obstructive Pulmonary Disease (COPD) (PFT)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Alpha-1 Foundation
ClinicalTrials.gov Identifier:
NCT01419158
First received: August 16, 2011
Last updated: January 18, 2012
Last verified: September 2011

August 16, 2011
January 18, 2012
January 2008
January 2010   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT01419158 on ClinicalTrials.gov Archive Site
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Prevalence of Alpha-1 Antitrypsin Deficiency in Chronic Obstructive Pulmonary Disease (COPD)
Targeted Detection of Alpha-1 Antitrypsin Deficiency in Patients Referred for Pulmonary Function Testing

Alpha-1 antitrypsin deficiency (AATD) is considered a rare genetic cause of chronic obstructive pulmonary disease (COPD) and liver disease. Recent data has suggested that AATD is not as rare as originally thought and undetected AATD may account for COPD in some patients. This study was designed to evaluate the frequency of undetected AATD in a population reporting to academic pulmonary function testing facilities who meet criteria for the diagnosis of COPD. All individuals meeting GOLD criteria for COPD will be consented and offered free testing for AATD. The results will help identify the percent of those with COPD who have undetected AATD.

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Observational
Observational Model: Case-Only
Time Perspective: Prospective
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Non-Probability Sample

Individuals reporting for pulmonary function testing who meet criteria for the diagnosis of chronic obstructive pulmonary disease

  • Alpha-1 Antitrypsin Deficiency
  • Chronic Obstructive Pulmonary Disease
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
3457
January 2010
January 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male and female adults at least 18 years of age able to understand and consent to the procedures of this protocol.
  • All races and ethnicities will be considered for this study.
  • Post-bronchodilator values for pulmonary function tests on the day of enrollment with an FEV1 < 80% of predicted and FEV1/FVC < 70% (at least GOLD stage II).
  • Subjects who have been tested for Alpha-1 in the past but do not know their genotype or phenotype may be included in this study.

Note: For the inclusion criteria the investigators will use the patient's GOLD status, based on percent predicted (FEV1 < 80% of predicted); however, after sending the absolute value of FEV1 to the Data Coordinating Center (DCC) the DCC will calculate the percent predicted using a standardized formula (NHANES III). For sites that do not use this predicted formula, the results obtained at the DCC may differ from those used for subject enrollment. (For example, a subject found to have an FEV1 of <80% at the study site could have an FEV1 > 80% when the DCC recalculates it). Enrollment will be based on the percent predicted at each study site. If necessary, the data from this small number of outliers will be analyzed separately.

Exclusion Criteria:

  • Subjects in whom post-bronchodilator spirometry is not performed.
  • Subjects whose ordering physician has specifically requested that his patients not be considered for enrollment.
  • Patients who have been tested for Alpha-1 in the past and know their genotype or phenotype.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States,   Puerto Rico
 
NCT01419158
PFT-001
No
Alpha-1 Foundation
Alpha-1 Foundation
Not Provided
Principal Investigator: Robert A Sandhaus, M.D., Ph.D. National Jewish Health
Alpha-1 Foundation
September 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP