Registry for Patients Undergoing Pulmonary Procedures
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|ClinicalTrials.gov Identifier: NCT01397292|
Recruitment Status : Terminated (funding/ enrollment)
First Posted : July 19, 2011
Last Update Posted : March 19, 2013
The purpose of this research study is to examine the safety, tolerability, and effectiveness of currently available pulmonary procedures when used to diagnose or treat different diseases.
This study will collect information that may influence the outcome of the procedure and identify factors that may affect the procedures yield or safety. The information will be entered into a registry or data storage.
|Condition or disease|
This is a retrospective and prospective data registry of all pulmonary diagnostic and therapeutic interventional pulmonary procedures at a single academic center. All pulmonary procedures upon completion will be entered into a database by the participating investigator performing the procedure. For both diagnostic and therapeutic cases, the data will require additional input 1-4 weeks after the procedure in order to place the diagnosis and follow-up data. Retrospective data will only be collected for patients that had their procedures prior to approval of this registry.
Study data will be collected and managed using REDCap (Research Electronic Data Capture) electronic data (CTSA Awared - Award Number UL1RR031990) capture tools hosted at Virginia Commonwealth University. REDCap is a secure, web-based application designed to support data capture for research studies.
The prison population will also be included in the registry in order to examine the effects of pulmonary procedures on a special population.
|Study Type :||Observational|
|Actual Enrollment :||220 participants|
|Official Title:||Registry Examining Retrospective and Prospective Data for Patients Undergoing Pulmonary Procedures|
|Study Start Date :||July 2011|
|Actual Primary Completion Date :||December 2012|
|Actual Study Completion Date :||December 2012|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01397292
|United States, Virginia|
|Virginia Commonwealth University|
|Richmond, Virginia, United States, 23060|
|Principal Investigator:||Hans J Lee, M.D.||Virginia Commonwealth University|