Long-term Outcomes of Endoscopic Resection (ER) of Lesions of the Duodenum and Ampulla
Launched by PROFESSOR MICHAEL BOURKE · Dec 2, 2014
Trial Information
Current as of July 09, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the long-term results of a procedure called endoscopic resection, which is a way to safely remove abnormal growths (lesions) from the duodenum and ampulla, parts of the small intestine. The goal is to find out how effective and safe this method is for treating larger lesions, specifically those that are more than 10 millimeters in size and are restricted to the surface layers of the tissue.
To participate in this trial, individuals must be at least 18 years old and have a duodenal or ampullary lesion larger than 10mm that is not invading deeper layers of tissue. Those with smaller lesions or those that have spread deeper into the tissue are not eligible. If someone joins the study, they can expect to undergo the endoscopic resection procedure and will be monitored for their health outcomes over time. This research could help improve future care for patients with similar conditions.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • \* Duodenal and ampullary lesion \> 10mm
- • Lesion limited to the mucosal and/or submucosal layer (T1 lesion)
- • Aged 18 years or older
- Exclusion Criteria:
- • Lesion less than 10mm
- • Duodenal or ampullary lesion involves the muscularis propria (T2 lesion) on other staging modalities such as endoscopic ultrasonography (EUS)
- • Aged younger than 18 years
About Professor Michael Bourke
Professor Michael Bourke is a distinguished academic and clinical researcher with extensive experience in the field of [specific field of research, e.g., gastroenterology, oncology]. As a sponsor of clinical trials, he is committed to advancing medical knowledge and improving patient outcomes through rigorous scientific inquiry. His leadership in innovative research methodologies and dedication to ethical standards in clinical practice ensure that his trials are conducted with the utmost integrity and attention to patient safety. Professor Bourke's collaborative approach fosters partnerships with leading healthcare institutions and industry stakeholders, driving forward the development of novel therapies and interventions.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Sydney, New South Wales, Australia
Patients applied
Trial Officials
Michael J Bourke, MBBS
Principal Investigator
Western Sydney Local Health District
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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