Navicam for Detection of Barrett's Esophagus

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age22+
SponsorMayo Clinic

About this trial

Using a non-invasive capsule system to achieve optimal viewing angles of the esophagus for detection of Barrett's esophagus

Eligibility criteria

Qualifiers

Adults greater than or equal to 22 years of age with or without Barrett's Esophagus

Presence of at least 1cm of salmon colored mucosa with corresponding biopsies showing intestinal metaplasia who are treatment naïve and undergoing surveillance Or

Chronic Gastro Esophageal Reflux Disease (GERD) patients with at least 3 additional risk factors that meet Barrett's Esophagus screening criteria per latest clinical guidelines

Disqualifiers

Inability to comprehend or read the consent form

Have an oropharynx, esophageal, or gastro-esophageal tumor

Ongoing symptoms of dysphagia

Presence of active clinically significant stricture

Trial design

Treatments tested in this trial

  • NaviCam Detachable String Capsule

Treatment groups

57 Participants
are divided into 3 treatment groups

Sponsors and collaborators