Barrett Esophagus
Conditions
Brief summary
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.
Detailed description
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.
Interventions
DEVICEPill cam
Patient is asked to swallow the esophageal capsule.
OTHEREGD
Patient will undergo standard EGD
Sponsors
Medtronic Spine LLC
Midwest Biomedical Research Foundation
Study design
Observational model
OTHER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* Patients age: ≥ 18 years * Patients with BE length ≥ 1cm undergoing upper endoscopy * Willingness to undergo both unsedated, capsule endoscopy and conventional EGD * Ability to provide written, informed consent and understand the responsibilities of trial participation
Exclusion criteria
* Coagulopathy with INR \> 1.5, thrombocytopenia with platelet counts \< 50,000 * Pregnant or planning a pregnancy during the study period * Dysphagia * Known esophageal diverticulum or stricture * Swallowing disorder * Known luminal, gastrointestinal stricture * History of esophageal, gastric surgery * Esophageal or GI motility disorder * Subject has a known history of unresolved drug or alcohol dependency that would limit ability to comprehend or follow instructions related to informed consent, post-treatment instructions, or follow-up guidelines * Known or suspected gastrointestinal obstruction, strictures, or fistulas based on the clinical picture or pre-procedure testing and profile. * Subjects with cardiac pacemakers or other implanted electromedical devices. * Anticipated magnetic resonance imaging within 1 week of capsule ingestion
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The overall diagnostic accuracy of capsule endoscopy in predicting the presence and extent of Barrett's esophagus in comparison to standard esophagogastroduodenoscopy | 1 year | The ability to accurately predict the presence of Barrett's esophagus by capsule endoscopy and standard EGD will be measured. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of Treatment related adverse events of capsule endoscopy in comparison to standard esophagogastroduodenoscopy | 1 year | Wireless capsule endoscopy is generally considered safe. Potential risks resulting from capsule endoscopy are reported low and may include discomfort while swallowing, accidental aspiration and capsule retention leading to small bowel obstruction and perforation. the investigator will measure tolerability of capsule endoscopy as well as standard endoscopy using visual analogue scale. |
Countries
United States
Outcome results
None listed