Chronic Granulomatous Disease Clinical Trial
Official title:
Diagnostic Efficacy of Virtual Bronchoscopy
This study will evaluate a new technique for examining the air passages of the lungs called
"virtual bronchoscopy." It involves using computed tomography (CT) images of the chest to
generate a 3-dimensional model of the walls of the trachea and bronchi (airway passages).
This non-invasive method lets doctors see small masses and areas of narrowing in the
passages without having to do surgery or pass a tube through them.
Patients with diseases of the air passages who are enrolled in an NIH clinical trial may
participate in this study, which requires having a CT scan. The patient lies on a table that
slowly slides into a hole in a donut-shaped X-ray machine (the scanner). Patients may have
to hold their breath several times during the procedure. Some patients may be given an
injection of a contrast agent through a catheter (thin tube) placed in an arm vein to
improve visibility of abnormalities. Patients may also be asked to breathe oxygen through
nasal prongs to allow them to hold their breath longer. The procedure usually takes 15 to 20
minutes.
Status | Completed |
Enrollment | 120 |
Est. completion date | November 2001 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Patients with Wegener's granulomatosis who are scheduled for fiberoptic bronchoscopy. Patients with cavitary lung diseases who are enrolled in protocols studying patients with Wegener's granulomatosis, chronic granulomatosis disease, host immune defects, mycobacterial infections, and Job's syndrome. Patients with bronchogenic carcinoma, other thoracic malignancies, or metastatic disease to the thorax. Patients will be selected from Clinical Center inpatient and outpatient population based on a clinical suspicion of pulmonary, mediastinal or bronchial disease, and are to have medically indicated chest CT. Written informed consent will be obtained from all patients and studies will only be done with the permission of the patient's attending physician. Patients will be drawn from the following protocols: 92-I-0186 93-I-0119 94-I-0149 95-I-0091 90-I-0086 76-I-0023 92-I-0255 93-I-0172 95-I-0177 Subjects must not be pregnant and be able to hold their breath for required periods of time. |
Endpoint Classification: Safety Study, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Warren G. Magnuson Clinical Center (CC) | Bethesda | Maryland |
Lead Sponsor | Collaborator |
---|---|
National Institutes of Health Clinical Center (CC) |
United States,
Summers RM, Feng DH, Holland SM, Sneller MC, Shelhamer JH. Virtual bronchoscopy: segmentation method for real-time display. Radiology. 1996 Sep;200(3):857-62. — View Citation
Summers RM, Shaw DJ, Shelhamer JH. CT virtual bronchoscopy of simulated endobronchial lesions: effect of scanning, reconstruction, and display settings and potential pitfalls. AJR Am J Roentgenol. 1998 Apr;170(4):947-50. — View Citation
Summers RM. Navigational aids for real-time virtual bronchoscopy. AJR Am J Roentgenol. 1997 May;168(5):1165-70. — View Citation
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