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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03764163
Other study ID # 199708651
Secondary ID 5R01HL064368
Status Completed
Phase Early Phase 1
First received
Last updated
Start date September 30, 1997
Est. completion date June 5, 2015

Study information

Verified date January 2019
Source University of Iowa
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research study is to develop CT scanning and image analysis techniques to help define and measure several key properties of the pulmonary system that cannot be obtained by other tests or exams.


Description:

Specifically, the investigators are interested in understanding the difference between the normal aging process and the events that lead to emphysema. Additionally, the investigators are interested in understanding the earliest signs (lung inflammation) of the disease process leading to three lung diseases, which include emphysema, fibrosis and sarcoidosis; all of which are described as "inflammatory lung diseases." The investigators will be using the data from this study to help define the normal values for the measured properties as well as deviation from normal values in smokers without defined lung disease and patients with inflammatory lung disease. The investigators believe that the analysis and scanning techniques being developed as part of this research will provide new and previously unavailable information on normal and diseased lungs so that ultimately the investigators can detect specific changes in the lungs due to a disease and measure any improvements in the anatomy and/or function of the pulmonary system after a patient has undergone treatment. This study involves research using X-Ray computed tomography (CT) scanner, which is similar to previous CT scanners but operates much faster and provides finer image detail.


Recruitment information / eligibility

Status Completed
Enrollment 341
Est. completion date June 5, 2015
Est. primary completion date June 5, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 89 Years
Eligibility Inclusion Criteria:

- Non smokers, age 20-29, 40-49, 60-69, 80-89, cannot have smoked more than 20 cigarettes in their lifetime

- Smokers, age 20-29, 40-49, 60-69, 80-89, currently smoking a minimum of 1 pack (20 cigarettes) per day, normal smokers and mild to moderate Chronic Obstructive Pulmonary Disease (COPD)

Exclusion Criteria:

- Allergies - no allergies to shellfish, eggs, iodine

- Medications - no medications (except for birth control) for in the 'normal' category

- No asthma - as self reported

- BMI (Body Mass Index) - must not exceed 32 or 100kg of weight

- No other radiology studies in the last 12 months

- No metal in lung field - no metal from larynx to stomach

- No known heart disease

- No known kidney disease or diabetes

- Must not be pregnant - subjects of childbearing potential with be given a urine pregnancy test

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Pulmonary Function Test
Spirometry, Diffusing Capacity of the Lungs (DLCO), Lung Volumes
CT Scans
volume scans, perfusion scan, ventilation scan
Behavioral:
Questionnaires
Human Subjects Questionnaire, Baseline Dyspnea Index, Chronic Respiratory Questionnaire
Diagnostic Test:
MRI
proton scans, hyperpolarized 3-Helium scan
Biological:
Xenon gas
ventilation CT scans

Locations

Country Name City State
United States University of Iowa Hospitals and Clinics Iowa City Iowa

Sponsors (3)

Lead Sponsor Collaborator
Eric A. Hoffman National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Normal lung aging assessed by CT imaging Normal aging process of the lungs compared to common smoking related lung diseases. up to 10 years
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