Clinical trial · Interventional
Eradicating Barrett's Esophagus Using Radiofrequency Ablation or a Novel Hybrid Argon Plasma Coagulation Technique
Eradicating Barrett's Esophagus Using Radiofrequency Ablation or a Novel Hybrid Argon Plasma Coagulation Technique (BURN)
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Closure due to the COVID-19 pandemic: Protocol specified procedures could not be followed resulting in unavoidable protocol deviations. Lower enrollment than expected. Competing COVID-19 studies at study sites. No ethical, scientific, safety issues.
Summary
Brief summary (as posted)
Lay summary: Barrett's Esophagus (BE) involves a change of the esophagus lining (BE epithelium) which in a small proportion of patients could be the starting point for the development of cancer (esophageal adenocarcinoma). Currently, there is evidence that this change is initiated by acid reflux from the stomach which then could progress in a stepwise manner from the healthy epithelium to cellular changes (intestinal metaplasia, low-grade and high-grade dysplasia) and finally to adenocarcinoma. Surgery is considered the standard therapy for this cancer which involves the risk of death and complications with quality of life impairments. New possibilities for treatment have evolved with endoscopic therapies which allow for treatment of early changes of the epithelium (intestinal metaplasia and dysplasia) prior to the occurrence of cancer using either argon plasma coagulation (APC) or radiofrequency ablation (RFA). Both are established methods for eradication of BE by thermal ablation of the BE epithelium using high frequency current (HF). More advanced BE epithelium with early visible cancers are being treated by endoscopic mucosal resection (EMR). After EMR the residual Barrett's epithelium can also be removed by ablation with RFA or APC. Currently radiofrequency ablation (RFA) has been suggested as the standard therapy for BE treatment. Although effective in the eradication of the BE epithelium after RFA treatment the re-appearance of BE epithelium and the occurrence of complications such as strictures causing swallowing impairments for food have also been observed in clinical studies. A recently developed method is Hybrid argon plasma coagulation (ablation) \[HybridAPC® (HAPC)\] which combines argon plasma coagulation (APC) with a fluid injection function by a water beam. The water beam allows to establish a fluid cushion (normal sterile saline) right beneath the BE-epithelium prior to thermal ablation thereby protecting the esophagus wall from heat during ablation of epithelium with APC. The goal of this randomized controlled study is to investigate if HAPC is non-inferior to RFA in the stricture-free eradication of the dysplastic BE epithelium.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Barrett's Esophagus | — | UNRESOLVED | — |
| High-grade Dysplasia in Barrett Esophagus | — | UNRESOLVED | — |
| Low Grade Dysplasia in Barrett Esophagus | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Hybrid argon plasma ablation (HAPC) | Device | — | UNRESOLVED |
| Radiofrequency ablation (RFA) | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Hybrid argon plasma ablation (HAPC)
- description
- Eligible participants will be randomized to receive ablation of dysplasia with Hybrid argon plasma coagulation (HAPC) after EMR of visible lesions (if present) has been performed as per standard of care.
- interventionNames
- Device: Hybrid argon plasma ablation (HAPC)
- type
- ACTIVE_COMPARATOR
- label
- Radiofrequency ablation (RFA)
- description
- Eligible participants will be randomized to receive treatment of dysplasia with RFA after EMR of visible lesions (if present) has been performed as per standard of care.
- interventionNames
- Device: Radiofrequency ablation (RFA)
Primary outcomes (1)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 86 Years
Show eligibility criteria text
Inclusion Criteria: * Age of 18-85 years (inclusive) * Dysplastic BE, confirmed by the central pathologist; specifically: * Low grade dysplasia documented on biopsy within 6 months of consent date or * High grade dysplasia documented on biopsy within 6 months of consent date * Barrett's extent of: C/M≥1 cm and C/M ≤ 6 cm using the Prague criteria \[C = circumferential extent of disease / M = maximum extent of disease\] * Ability to provide written and informed consent Exclusion Criteria: * Barrett's extent of: C/M \<1 cm or a C/M-value \> 6 cm using the Prague criteria * Prior EMR (endoscopic mucosal resection) for G3/G4; L1; V1; R1 (vertical margin only) or submucosal invasion; * Presence of endoscopically visible abnormalities at the time of initial study treatment with HAPC or RFA. These participants can undergo EMR and then continue in the trial after a suitable healing period, provided randomization can occur within 90 days of consent. * Presence of invasive cancer on biopsy * Known pregnancy or plans to become pregnant * Complete eradication is not considered a relevant treatment goal or in whom additional treatment is contraindicated; * pre-existing significant esophageal pain or dysphagia; * BE \>80% has been resected by EMR; * incomplete wound healing 3 months post-EMR despite adequate PPImedication; * Prior ablative therapy in the esophagus but prior EMR allowed * Active esophagitis or stricture precluding passage of scope * Presence of esophageal varices * Anticoagulant therapy (apart from aspirin or NSAIDS) that cannot be discontinued prior to therapy or uncorrectable hemostatic disorders * Life expectancy less than 2 years * Previous gastrectomy or other gastric surgery other than uncomplicated fundoplication
References
Publications (0)
Data not yet available