Pulmonary Coin Lesion Clinical Trial
— ALOSPNDYOfficial title:
A Pilot Prospective Study Evaluating the SPiN Drive(TM)Electromagnetic Tip Tracked Devices Used in Diagnostic Bronchoscopy
Verified date | July 2014 |
Source | Veran Medical Technologies |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The objective of the prospective, multi-center study is to evaluate the ease of use and effectiveness of the SPiN Drive Electromagnetic (EM) Tip Tracked Steerable Devices as a method of sampling subsegmental, less than 3.0 cm, lung lesions through the airway, and beyond the bronchus. Measures of diagnostic yield will be compared to the diagnostic yield of similar published historical controls using conventional bronchoscopy.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | November 2011 |
Est. primary completion date | November 2011 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 50 Years and older |
Eligibility |
Inclusion Criteria: - Subject provides informed consent - Subject is older than 50 years of age with 50% of patients at least 65 years of age - Patient has a minimum of 20 pack years - Subject scheduled to undergo conventional bronchoscopy as part of their standard medical care - Subject has radiographically confirmed sub-segmental peripheral < 3.0 cm lung lesions - A negative pregnancy test in women of child-bearing potential - Subject is willing and able to return for all required follow-up - Subject is mentally capable of following study directions Exclusion Criteria: - Subject has pacemaker, implantable cardioverter, and/or defibrillator - Subject has any disease or condition that interferes with safe completion of initial or follow-up assessments - Pregnant or nursing female subjects, or female subjects of child bearing potential who refuse to take a pregnancy prior to their enrollment in this study - Concurrent participation in another study involving investigational drugs or investigational medical devices - Inability to read and understand the necessary study documents |
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Diagnostic
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Veran Medical Technologies | Institute for Quality Resource Management |
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Diagnostic yield of a subsegmental pulmonary lesion of less than 3.0 cm. | Biopsy samples will be sent to the lab for analysis of the presence, absence, or identification of an occult particulate taken from the patient's lung. Patients with a negative biopsy result will be followed if recommended for another intervention and if recommended to watchful waiting. Follow up outcomes will be included in the outcome measures. | Within 1 week | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01730365 -
Optical Detection of Malignancy During Percutaneous Interventions
|
N/A |