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Prophylactic Octreotide to Prevent Post Duodenal EMR and Ampullectomy Bleeding

Adenoma Clinical Trial

Official title:
Prophylactic Octreotide to Prevent Post Duodenal EMR and Ampullectomy Bleeding

Clinical Trial Summary

Our hypothesis is that prophylactic administration of 5 days of Octreotide following EMR or ampullectomy in patients with duodenal and ampullary adenomas greater than or equal to 10mm.

Clinical Trial Description

Inclusion Criteria:

Duodenal or ampullary adenoma greater than or equal to 10mm. Duodenal or ampullary adenoma that is suitable for endoscopic mucosal resection.

Medically fit for anesthesia, endoscopy, and EMR Able to provide Informed Consent 18 years or older, male and female

Exclusion criteria:

Duodenal or ampullary adenoma <10mm Duodenal or ampullary adenoma that is not suitable for endoscopic mucosal resection Medically unfit for anesthesia, endoscopy, or EMR Unable to provide Informed Consent Less than 18 years old Allergy to Octreotide ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02032784
Study type Interventional
Source AdventHealth
Contact
Status Terminated
Phase Phase 4
Start date March 2014
Completion date July 6, 2020
View Details
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