Prospective Study to Compare the Efficacy of E.G.Scan to Detect Barrett's Esophagus Compared With Standard Endoscopy
Completed · Not applicable
Conditions studied: Barrett's Esophagus
In brief
The purpose of this study was to evaluate whether a disposable nasal endoscope called "E.G. Scan II" will visualize the esophagus as well as the standard test, sedated endoscopy.
Key facts
- Study ID
- NCT02066233
- Run by
- Mayo Clinic
- People needed
- 100
- Starts
- 2014-03-01
- Expected to finish
- 2016-03-01
- Last updated by the study team
- 2017-07-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Adult participants aged 18 years or above who are scheduled for routine upper GI endoscopy for Barrett's Esophagus surveillance, varices surveillance and dyspepsia.
- Able and willing to give informed consent.
You may not qualify if…
- Patients known to be intolerant to endoscopy.
- Patients with frequent epistaxis.
- Patients not clinically fit for endoscopy as judged by their care team.
- Pregnant women.
- Patients with allergy/sensitivity to Simethicone (Mylicon), Phenylephrine, Lidocaine nasal spray, Benzocaine spray (Topex)
- Use of anticoagulants or antiplatelets.
Where it is running
- Mayo Clinic — Rochester, Minnesota, United States
Full record on ClinicalTrials.gov
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