Not yet recruiting NCT07337980
A Study on the Safety and Effectiveness of Endoscopic Intracavitary Submucosal Dissection for Gastric Extracavitary-Type Submucosal Tumors
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Extraluminal growing stromal tumors treated endoscopically.
- Who it may be relevant to
- Registry conditions: Interstitialoma, Endoscopic Surgery. Basic parameters: 18 years — 80 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The aim of this study is to explore the safety and efficacy of endoscopic surgery in the treatment of extraluminal growing stromal tumors
Detailed description
The aim of this study is to explore the safety and efficacy of endoscopic surgery in the treatment of extraluminal growing stromal tumors
Interventions
- Procedure Extraluminal growing stromal tumors treated endoscopically
To observe the safety and efficacy of endoscopic treatment of extraluminal growing stromal tumors
Primary outcome measures
- Complete resection rate [Time frame: 12 months]
Secondary outcome measures (1)
- Recurrence-free survival [Time frame: 12 months]
Eligibility criteria
Inclusion criteria
- (1) CT scan showed extramural protrusion of the stomach (2) ultrasonic endoscopy revealed submucosal tumors with extra-gastric growth; (3) patients received ESD/EFTR or surgical treatment
Exclusion criteria
- (1) patients had malignant tumors in the stomach or had undergone stomach surgery (2) follow-up records were incomplete.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07337980 · GI of Zhongda Hospital