Esophageal Cancer Clinical Trial

“Acetic Acid Chromoendoscopy in Barrett’s Esophagus Surveillance

Summary

Neoplasia in Barrett's esophagus could be missed during routine random biopsies. We propose a study using chromoendoscopy with Acetic Acid to increase the yield of biopsies in detecting neoplasia.

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Full Description

Neoplasia in Barrett's esophagus is often focal and can be missed by nontargeted biopsies alone. In recent years, various advanced endoscopic techniques have been utilized, but with varying success rates. Narrow-band imaging, trimodal imaging, spectral imaging and i-scan are technologies that are manufacturer dependent with limited varying success rates and have financial implications. At our institution, narrow band imaging is routinely utilized as a diagnostic tool for detecting Barrett's esophagus. Acetic acid is a commonly available dye that has been used in the detection of neoplasia in Barrett's esophagus.

This study is aimed to prove the effectiveness of acetic acid chromoendoscopy in our Barrett's esophagus surveillance population. The goal is to compare the neoplasia yield of acetic acid chromoendoscopy with that of standardized random biopsy protocol. The sensitivity and specificity for neoplasia detection by these two methods will also be analyzed.

Investigators plan to conduct this prospective randomized study for a period of one and a half years (beginning August 1, 2015, ending February 29, 2016). Based on data from 2014, we anticipate to enroll approximately 185 patients. All gastroenterologists (with privileges at Doctors Hospital at Renaissance) will participate in this study. Patients will be randomized to either acetic acid chromoendoscopy or current standard of care (standardized random biopsy protocol utilizing narrow band imaging). Random biopsies from both protocols and targeted biopsies (if identified) will be obtained and submitted to pathology department. These will be reviewed independently by two pathologists. Any discordant results will be reviewed by an outside expert pathologist. Statistical data analysis will be performed utilizing Datadesk XL software.

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Eligibility Criteria

Inclusion Criteria:

Patients 18 years and older
Previous diagnosis of Barrett's esophagus, confirmed by pathology.

Exclusion Criteria:

Patients diagnosed with any level of dysplasia on previous esophageal biopsies.
Patients who had esophageal therapy with Halo radiofrequency ablation in the past, or esophagectomy.
History of allergy to Acetic Acid
History of esophageal dysplasia or cancer
Esophageal ulcerations
Esophageal Candida
Esophageal Varices
Patients with active esophagitis
Patients who cannot provide a valid consent
Patients who are currently pregnant

Study is for people with:

Esophageal Cancer

Phase:

Phase 2

Estimated Enrollment:

60

Study ID:

NCT02614703

Recruitment Status:

Terminated

Sponsor:

DHR Health Institute for Research and Development

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There is 1 Location for this study

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Doctors Hospital at Renaissance/Endoscopy Department
Edinburg Texas, 78539, United States

How clear is this clinincal trial information?

Study is for people with:

Esophageal Cancer

Phase:

Phase 2

Estimated Enrollment:

60

Study ID:

NCT02614703

Recruitment Status:

Terminated

Sponsor:


DHR Health Institute for Research and Development

How clear is this clinincal trial information?

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