Barrett Esophagus Clinical Trial
Official title:
Evaluation of Performance Characteristics of Capsule Endoscopy With PillCam UGI Capsule Compared to Standard Endoscopy for Screening of Barrett's Esophagus: A Prospective Tandem Study
This study is to examine the benefits of newly designed capsule with enhanced frame rate and wide angle compared to standard endoscopy, which may help enhance detecting esophageal diseases that otherwise may have been out of vision in the standard endoscopy, ultimately decreasing healthcare costs.
This is a pilot, single center, prospective, tandem study. All veteran patients with
Barrett's esophagus scheduled for an upper EGD at Veterans Affairs Medical Center (Kansas
City, MO, USA) for check-up of BE will be asked to swallow the pillcam prior to an EGD. A
member of the research team will approach a potential subject to discuss participation in the
study, including background of the proposed study, inclusion and exclusion criteria, benefits
and risks of the procedures and follow-up. If this is of interest to the subject, the
informed consent form is discussed and presented. The subject must sign the consent form
prior to enrollment. This form will have prior approval of the study site's Institutional
Review Board (IRB). Failure to obtain informed consent renders the subject ineligible for the
study
Eligible subjects at the participating institution who meet the inclusion criteria for this
study will be offered the opportunity to participate in this clinical trial. To ensure that
subjects are approached for potential study participation without bias, a Subject Screening
Log will be maintained. This Log will track the basic demographic information of each subject
approached for clinical trial inclusion and the resulting reason for exclusion from the
clinical study if applicable.
The duration of the study is expected to be approximately 12 months. Enrollment of Study
patients will cease when approximately 20 patients have been enrolled.
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