Multi-center Clinical Study to Evaluate the C2 CryoBalloon Focal Ablation System (NCT02514525) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Multi-center Clinical Study to Evaluate the C2 CryoBalloon Focal Ablation System
United States150 participantsStarted 2016-03
Plain-language summary
To evaluate the efficacy and safety of the CryoBalloon Focal Ablation System for the treatment of previously-untreated ("treatment naïve") Barrett's Esophagus (BE)
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Low- or high-grade non-nodular, previously untreated ("treatment naïve") dysplastic BE, confirmed by histopathological analysis. If nodular BE or Intramuscosal Cancer (ImCA) is identified during patient screening, this may be treated with Endoscopic Mucosal Resection (EMR) ≥6 weeks prior to treatment under this protocol. If previous EMR was performed, follow-up endoscopy must be negative for nodular BE. Patients with ImCA must be at low risk for recurrence, confirmed by EMR pathology results negative for positive margin, poorly differentiated carcinoma, and lymphovascular invasion.
* BE length ≤6cm excluding visible BE islands, and Prague Classification C ≥0 / M ≥1
* Older than 18 years of age at time of consent
* Operable per institution's standards
* Provides written informed consent on the approved informed consent form
* Willing and able to comply with study requirements for follow-up
Exclusion Criteria:
* Non-dysplastic or indefinite for dysplasia BE, confirmed by histopathological analysis
* Esophageal stenosis/stricture preventing advancement of a therapeutic endoscope (patients may have the stenosis/stricture dilated and then be treated with CryoBalloon ablation under this protocol at a subsequent procedure ≥2 weeks later)
* Symptomatic untreated strictures
* Any endoscopically-visualized abnormalities such as ulcers, masses or nodules. Neoplastic nodules must first be treated with EMR ≥6 weeks prior to planned treatment under this protocol.
*…
What they're measuring
1
Incidence of serious, CryoBalloon Ablation System-related adverse events
Timeframe: 12 months
2
Percentage of patients with baseline LGD who have complete eradication of all dysplasia
Timeframe: 12 months
3
percentage of patients with baseline HGD who have complete eradication of all dysplasia
Timeframe: 12 months
4
percentage of all treated patients who have complete eradication of all dysplasia (CE-D)