BENITIONSClinical Trial Intelligence

CryoBalloon Ablation for Treatment of Duodenal Adenomas

N/A Completed NCT03847636

ConditionDuodenal Adenomas, Familial Adenomatous Polyposis
PhaseN/A
SponsorJohns Hopkins University
StatusCompleted
Enrollment33 participants
InterventionsCryoBalloon ablation
Start dateMay 13, 2019
Completion dateJun 1, 2025
Results postedAug 4, 2026

Summary

This multicenter prospective non-randomized interventional study (clinical trial) that will assess the safety and efficacy of cryoballoon ablation treatment using the C2 Cryoballoon device (Pentax Medical Corporation) as an alternative primary treatment modality for sporadic and familial nonampullary nonpolypoid (flat) duodenal adenomas.

Safety of CryoBalloon Ablation in Treating Non-ampullary Non-polypoid Duodenal Adenomas (DAs) as Assessed by Participants With Adverse Events

1 year · Participants

Individuals With Duodenal Adenomas12 Participants

Participants With Complete Eradication of DA

1 year · Participants

Individuals With Duodenal Adenomas23 Participants

Open in BENITIONS View on ClinicalTrials.gov

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