MedPath

Hybrid Argon Plasma Coagulation (Hybrid-APC) for the treatment of Barrett*s esophagus with Low-Grade, High-Grade Intraepithelial Neoplasia or after Endoscopic Resection for Early Neoplasia

Completed
Conditions
Barrett dysplasia precancerous
10017990
Registration Number
NL-OMON40133
Lead Sponsor
Academisch Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

a) Patients in the age of 18-85 years
b) Residual BE (defined as columnar lined esophagus with intestinal metaplasia) after prior ER (max 3 ER procedures) for HGD or mucosal cancer, irrespective if the residual BE harbors NDBE, LGD or HGD, OR patients with a BE without prior ER and a confirmed histological diagnosis of HGD or LGD.
c) Written informed consent.

Exclusion Criteria

a) BE with a C-value <1 or a C-value >10 cm
b) Prior ER for G3/G4; L1; V1; R1 (vertical margin only) or submucosal invasion;
c) Presence of endoscopically visible abnormalities at the time of initial APC treatment (additional ER is allowed);
d) Presence of cancer in random biopsies obtained at the mapping endoscopy, 8-12 weeks before initial APC treatment;
e) Pregnancy
f) Patients in whom complete eradication is not considered a relevant treatment goal or in whom additional treatment is contraindicated;
g) Patients in whom >80% of the BE has been resected by ER;
h) Patients with incomplete wound healing 3 months post-ER despite adequate PPI-medication;
i) Prior ablative therapy in the esophagus;
j) Significant esophageal stenosis prior to initial APC treatment defined as a stenosis that can not be passed by a therapeutic endoscope or a stenosis that has been dilated endoscopically before.
k) Presence of esophageal varices
l) Anticoagulant therapy (apart from aspirin or NSAIDS) that can not be continued prior to APC or hemostatic disorders
m) Life expectancy less than 1 year

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>1. Complete eradication of BE<br /><br>2. Complete eradication of neoplasia</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>1. Number of Hybrid-APC treatment sessions (resection not considered)<br /><br>2. Early and late postoperative complications (retrosternal pain, dysphagy,<br /><br>odynophagy, fever bleedings, perforation, stenosis, mortality) and required<br /><br>therapies for the treatment of stenosis (rate of bougie applications, number of<br /><br>dilatations applied to each patient)<br /><br>3. Recurrence rate of BE and neoplasia within one year follow-up in both groups<br /><br>4. Predictive factors for treatment success<br /><br>5. Neoplastic progression under treatment</p><br>
© Copyright 2025. All Rights Reserved by MedPath