Optical Frequency Domain Imaging (OFDI) Surveillance and Image Guided Biopsy of the Esophagus

Not Applicable

Completed

Brief Summary: The specific aim of this study is to determine the feasibility of marking target pathologic locations identified on Optical Frequency Domain Imaging (OFDI) datasets using superficial cautery marks of the esophagus that are visible by endoscopy for subsequent guidance of biopsy.

Detailed Description: Twenty four consenting patients undergoing esophagogastroduodenoscopy (EGD) surveillance following a confirmed diagnosis of Barrett's esophagus will be recruited at Massachusetts General Hospital (MGH) . Along with Optical Frequency Domain Imaging (OFDI) imaging and cautery marking for targeted biopsy, the patients will undergo a standard of care clinical Esophagogastroduodenoscopy (EGD) procedure including endoscopic random biopsy. This study requires the use of a balloon catheter which is a commonly used technique and is accepted in clinical practice for dilation of esophageal and colonic strictures and for photodynamic therapy.

Once in position, the OFDI tissue marking laser will be activated by the physician. The physician will control the marking and make two marks of a duration of 2 seconds each. The 2 seconds time period will limit the tissue effects to only the superficial layers of the esophageal mucosa.

It is expected that the total experimental time including insertion and inflation of the OFDI balloon catheter, OFDI imaging, tissue marking, and removal of the OFDI balloon will add approximately 15 minutes to the total length of the EGD.

Recruitment & Eligibility

Inclusion Criteria

Patients undergoing an EGD for Barrett's esophagus surveillance with a prior confirmed Barrett's segment at least 1 cm in length
Patients must be over the age of 18
Patient must be able to give informed consent
Women with child bearing potential must have a negative pregnancy test prior to procedure

Exclusion Criteria

Patients on anti-platelet and anti-coagulation medications and NSAIDS at the time of procedure
Patients with a history of hemostasis disorders
Patients that are pregnant
Patients with esophageal strictures

Arm && Interventions

Group	Intervention	Description
MGH OFDI marking and imaging	MGH OFDI marking	OFDI imaging

Primary Outcome Measures

Name	Time	Method
Number of Subjects in Which the Targeted Locations Identified Through OFDI Imaging Correlates With the Biopsies.	day 1, during diagnostic procedure	Determination of the feasibility to mark targeted pathologic locations identified through OFDI imaging using superficial cautery marks.Verification by endoscopy and utilization of the marks for biopsy guidance.Images will be analyzed and compared to biopsies of the correlated marked tissue.

Secondary Outcome Measures