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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: Netherlands Trial Register
Last refreshed on: 27 May 2013
Main ID:  NTR2510
Date of registration: 03/09/2010
Primary sponsor: Academic Medical Center (AMC)
Public title: Improving practicality of radiofrequency ablation for eradication of Barrett's mucosa: A randomized trial comparing two different treatment regimens for focal ablation using the HALO90 System.
Scientific title: Improving practicality of radiofrequency ablation for eradication of Barrett's mucosa: A randomized trial comparing two different treatment regimens for focal ablation using the HALO90 System. -
Date of first enrolment: 1/10/2008
Target sample size: 46
Recruitment status: recruiting
URL:  http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=2510
Study type:  intervention
Study design:  Randomised: Yes; Masking: Double; Control: Active; Group: Parallel; Type: 2 or more arms, randomized  
Countries of recruitment
The Netherlands
Contacts
Name: J.J.G.H.M.  Bergman
Address:  Academic Medical Center Bldg. C2-210, Meibergdreef 1105 AZ Amsterdam The Netherlands
Telephone: +31 (0)20 5669111
Email: j.j.bergman@amc.uva.nl
Affiliation: 
Name: J.J.G.H.M.  Bergman
Address:  Academic Medical Center Bldg. C2-210, Meibergdreef 1105 AZ Amsterdam The Netherlands
Telephone: +31 (0)20 5669111
Email: j.j.bergman@amc.uva.nl
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: 1. Scheduled HALO90 ablation for BE (with or without neoplasia) after prior circumferential ablation using the HALO360 System for BE with flat low-grade dysplasia (LGD) or high-grade dysplasia (HGD) or for BE (with or without neoplasia) after prior endoscopic resection (ER) for lesions containing HGD or and early cancer;

2. One or more BE islands with a minimum size of 5-mm;

3. Written informed consent.



BE islands selection/Inclusion criteria:

Maximum size ≤4 adjacent HALO90 applications and <50% of the circumference.



Exclusion criteria: 1. Patients with endoscopically active inflammation in the treatment zone;

2. Esophageal stenosis preventing advancement of the endoscope with the HALO90 catheter.



BE islands selection/Exclusion criteria:

1. Prior treatment of the selected islands with HALO90 ablation;

2. Endoscopically visible abnormalities in one of the selected islands;

3. Patients unable to give informed consent.


Age minimum:
Age maximum:
Gender:
Health Condition(s) or Problem(s) studied
Barrett's esophagus, Barrett's neoplasia, Barrett's dysplasia, Radiofrequency ablation, Intestinal metaplasia, Intraepithelial neoplasia

Intervention(s)
Focal endoscopic radiofrequency ablation using the HALO90-catheter of the HALO System: Standard or simplified regimen:

Prior to ablation the exact location of islands were registered: Distance to biteblock (cm) and the o'clock position, to by able to relocalize the treatment zone at follow-up endoscopy after 2 months.



Standard regimen:

After mapping and randomization the Barrett?s segment is flushed with the mucolytic agent acetylcysteine (1%) followed by flushing with tap water. The endoscope is removed and the proximal esophagus is thoroughly inspected to exclude the presence of a Zenker?s diverticulum that may make subsequent introduction of the HALO90 cap difficult or dangerous.
The HALO90 cap is attached to the tip of the endoscope at the twelve o?clock position and introduced into the distal esophagus. Visible islands are then treated with 2x15 J/cm2 (40 Watt)): the cap is brought into close contact with the target area and is then activated. The endoscope and the cap are kept in position and immediately a second ablation of the same area is performed. After ablation of an island, the endoscope is gently removed from the mucosa and rotated to remove the coagulum by suctioning through the endoscope. If the squamocolumnar junction (SQJ) has an irregular appearance the SQJ is treated circumferentially, allowing an overlap of 5-10 mm between the adjacent ablations. After all islands and Z-line have been ablated in this manner, the necrotic debris is cleaned off by a combination of suctioning and irrigating tap water. In addition, the HALO90 cap can be used to gently push off the coagulum from the ablation zone. Subsequently, the ablated areas are cleaned by vigorous flushing of water through a spraying catheter. After emptying the stomach, the endoscope is removed, the HALO90 electrode is cleaned and then reintroduced to ablate all treated areas again with 2x15 J/cm2 (40 Watt).



Simplified regimen:

In the sim
Primary Outcome(s)
Rate of complete removal of BE islets (completely remove yes/no), as scored by the endoscopist (blinded for the allocation of the islands but nor the location of the islands that were randomized and treated) after 2 months as scored during the endoscopy using a standard case record form.
Secondary Outcome(s)
1. Percentage of endoscopically visual surface regression of BE epithelium after 2 months as scored by the endoscopist blinded to the treatment regimen during the endoscopy using a standard case record form, by a study monitor;

2. Number of introductions of the ablation device and endoscope as scored during the endoscopy using a standard case record form by a study monitor;

3. Complications as assessed by a telephone interview one or two days after the procedure and by registration using a standard case record form.
Secondary ID(s)
08/263
Source(s) of Monetary Support
BARRX Medical, Sunnyvale, CA, USA
Secondary Sponsor(s)
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