CryoBalloon Ablation for Treatment of Duodenal Adenomas
N/A
Completed
NCT03847636
| Condition | Duodenal Adenomas, Familial Adenomatous Polyposis |
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| Phase | N/A |
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| Sponsor | Johns Hopkins University |
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| Status | Completed |
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| Enrollment | 33 participants |
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| Interventions | CryoBalloon ablation |
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| Start date | May 13, 2019 |
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| Completion date | Jun 1, 2025 |
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| Results posted | Aug 4, 2026 |
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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 Adenomas | 12 Participants |
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Participants With Complete Eradication of DA
1 year · Participants
| Individuals With Duodenal Adenomas | 23 Participants |
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Open in BENITIONS
View on ClinicalTrials.gov
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