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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05930860
Other study ID # 4349
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 12, 2021
Est. completion date December 12, 2031

Study information

Verified date February 2023
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact Federico Barbaro
Phone 3921101013
Email federico.barbaro@policlinicogemelli.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Endoscopic submucosal dissection (ESD) is the technique that has replaced surgery in the treatment of early neoplastic lesions of the stomach (LNPS). ESD of LNPS allows: a) less invasiveness compared to surgery; b) greater chances of "en bloc" resection and R0 resection compared to mucosectomy for lesions larger than 15 mm. Recent 2015 ESGE guidelines provide precise recommendations for the use of ESD in the treatment of LNPS, but Italy lacks prospective data on the efficacy and safety of ESD in a large sample of patients. A multicenter prospective observational study to create a database on the use of ESD in LNPS is essential to provide information regarding the efficacy and safety of ESD in Italy. This database would also provide information regarding the criteria applied in the use of ESD in the treatment of early gastric neoplasia


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 12, 2031
Est. primary completion date December 12, 2024
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age > 18 years old - Endoscopic and histologic diagnosis of gastric superficial neoplasm that can be treated by ESD according to ESGE guidelines. - Gastric neoplasm outside of latest ESD guidelines criteria in patients unfit for surgery Exclusion Criteria: - Final diagnosis of non neoplastic lesion. - Gastric neoplasm outside of latest ESD guidelines criteria in patients fit for surgery - Evidence of muscolar layer invasion or limph nodes or other organs metastasis at EUS or TC when performed.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Endoscopic Submucosal Dissection
Endoscopic Submucosal Dissection

Locations

Country Name City State
Italy Digestive Endoscopy Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS Rome

Sponsors (1)

Lead Sponsor Collaborator
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary En bloc resection rate removal of the lesion into a single piece. 10 years
Primary R0 resection rate complete removal of the tumor with histologically lateral and vertical margins of the specimen free from dysplasia 10 years
Primary Curative resection rate R0 resection with combined microstaging parameters not suggestive for high metastatic potential risk. 10 years
Primary Complication rate bleeding, perforation and stenosis. 10 years
Primary Recurrence rate dysplastic tissue at the site of resection at follow-up endoscopy. 10 years
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