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The Effect of Ablation Therapy on Barrett's Esophagus

The Effect of Ablation Therapy on Barrett's Esophagus

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00587314
Acronym
ablation IN BE
Enrollment
600
Registered
2008-01-07
Start date
2004-01-01
Completion date
2029-01-01
Last updated
2026-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Barrett's Esophagus, Early Esophageal Adenocarcinoma

Keywords

Photodynamic Therapy, Barrett's Esophagus, Early Esophageal Adenocarcinoma

Brief summary

To assess the effect of ablative therapy (Photodynamic Therapy or Radiofrequency ablation ) on Barrett's Esophagus

Detailed description

To assess the effect of ablation therapy on Barrett's esophagus. Proposal Ablation therapy is an FDA approved treatment to decrease cancer risk in Barrett's esophagus mucosa. This is being performed in our Barrett's Esophagus Unit on a regular basis. However, the longterm outcomes of this therapy is not established and there are patients who have been treated who later re-develop Barrett's mucosa. This study will allow us store tissue samples that can later be used to assess the effect of ablative therapy on Barrett's esophagus.

Interventions

OTHERBiopsy

Biopsies for research purposes will be obtained when returning for clinically indicated surveillance of Barrett's Esophagus

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Patients who have had or qualify for ablation therapy for treatment of their barrett's esophagus with high grade dysplasia or early esophageal adenocarcinoma * Ability to provide informed consent

Exclusion criteria

* Eastern Cooperative Oncology Group performance status 3 or 4 * Inability to tolerate endoscopic procedures * Pregnancy: Females of child-bearing age will be screened with pregnancy test.

Design outcomes

Primary

MeasureTime frameDescription
Response to treatmentat time of surveillance intervalspresence of persistent or recurrence of barrett's esophagus and/or dysplasia

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORCadman Leggett, MD

Mayo Clinic

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026