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Completed

NCT Number: NCT01360541

Radiofrequency Ablation for Barrett Oesophagus With Low Grade Dysplasia

Radiofrequency ablation versus endoscopic surveillance in the management of low grade dysplasia in Barrett oesophagus: a multicentric randomised controlled trial.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Gastroenterology and Endoscopy department, Cochin Hospital

Paris, 75014, France

About this study

Background: The occurrence of low grade dysplasia (LGD) in Barrett oesophagus (BE) is known as a pre-cancerous state. Current recommendation in case of LGD is a close endoscopic surveillance every 6 to 12 month and continuous Proton pomp inhibitor (PPI) treatment. Endoscopic radiofrequency ablation (RFA) has been demonstrated as an efficient treatment to eradicate high grade dysplasia (HGD) and most of LGD and BE.

Main aim of this study: To demonstrate that the prevalence of patients with LGD 3 years after a RFA treatment is lower than in a surveillance group.

Patients & Methods: French multicentric randomized controlled trial for patients with BE with confirmed LGD: RFA vs endoscopic surveillance.

120 patients are planned to be included for at least 40 patients randomized in each group.

Primary endpoint: Prevalence of LGD in each group 3 years after randomization

Secondary endpoints:

  • Prevalence of LGD in each group 1 and 5 years after randomization
  • Rate of complete eradication of BE at 1, 3 and 5 years after randomization
  • Incidence of HGD and adenocarcinoma at 3, 5 years after randomization
  • Rate of complications in RFA group after randomization
  • Cost - efficacy comparison of the 2 strategies

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BE with certain LGD in at least one endoscopic biopsy sample
  • BE with maximal length of 12cm (Prague classification ≤ C12)
  • BE with minimal length of 1cm circumferentially or 3cm in case of a unique zone (Prague classification ≥ C1 or C0M3)
  • Patients aged between 18 and 80 years
  • Patients' consent for study enrollment
  • No contra-indications to general anaesthesia
  • Patients ability to take PPI oral medication
  • Patient affiliated to a social security system
  • No pregnancy and active contraceptions for women in age to procreate
  • In case of previous endoscopic mucosal resection for HGD in BE: at least one year of surveillance and 2 biopsy series with LGD without HGD

Exclusion criteria

  • BE length > 12cm or < 1cm circumferentially (< C1) or < 3cm focally (<M3)
  • HGD or adenocarcinoma needing a specific endoscopic or surgical treatment
  • Active peptic oesophagitis (Savary III or IV)
  • Presence of surgical staples on the area to be treated
  • Radiation oesophagitis of radiotherapy whose field includes the lower oesophagus
  • previous oesophagus cancer
  • previous endoscopic destruction treatment such as photodynamic therapy or plasma argon coagulation
  • previous Heller surgery
  • oesophagus stenosis
  • oesophagus varices
  • oesophagus pathology associated with sclerodermia
  • Severe coagulation disorders or thrombopenia
  • Anaesthesia contra-indications (ASA 4)
  • Hypersensitivity to fluorescein or any component of the fluorescein
  • Life expectancy < 2 years
  • Disability to take PPI oral medication or follow the protocol surveillance Schedule

Treatment and study plan

Endoscopic radiofrequency ablation

Procedure

HALO device Use of HALO 360° device for the fist procedure and possible use of HALo 90° device for further treatment sessions Treatment zone of 12cm high maximum. Energy delivered 10 J/cm², power 300W

Endoscopic surveillance

Other

Upper gastro-intestinal endoscopy every 6 to 12 month under propofol sedation with acetic acid magnification of mucosa and multiple biopsy samples.

Primary outcomes

  1. Prevalence of low grade dysplasia 3 years after randomization

    Time frame: 3 years after randomization

Secondary outcomes

  1. Prevalence of low grade dysplasia in each group

    Time frame: 1 and 5 years after randomization

  2. Rate of complete eradication of Barrett oesophagus

    Time frame: 1, 3 and 5 years after randomization

  3. Incidence of high grade dysplasia and adenocarcinoma

    Time frame: 3, 5 years after randomization

  4. Cost - efficacy comparison of the 2 strategies

    Time frame: 5 years

  5. Rate of complications in radiofrequency ablation group

    Time frame: 5 years after randomization

  6. Detection rate of dysplasia and Barrett's oesophagus with the confocal endomicroscopy technique

    Time frame: before treatment, during treatment (Month 3, Month 6, Month 9, Month 12) and after treatment (1, 3 and 5 years after randomization)

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Collaborators

  • URC-CIC Paris Descartes Necker Cochin

Registry information

Official study title

Endoscopic Radiofrequency Ablation for Barrett Oesophagus With Low Grade Dysplasia: a Randomised Controlled Trial vs Endoscopic Surveillance

Acronym: RF-DBG

Important dates

Study start
2010
Primary completion
2018
Study completion
2018
First posted
May 25, 2011
Registry last updated
Sep 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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