Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:58 AM
Ignite Modification Date:
2025-12-24 @ 11:58 AM
NCT ID:
NCT06840561
Eligibility Criteria:
Inclusion Criteria:
* staged as cT1aN0M0 or cT1bN0M0 before surgery via magnifying endoscopy, endosonography, CT, or PET/CT;
* refuse conventional surgery and CRT and got ESD as first-line treatment;
* mucosal defect measured by a circular protractor and reached more than three-quarters of the circumference of the esophageal lumen including whole circumference after ESD surgery;
* meet the minimum follow-up period of three months;
* signed the consent before ESD;
* If extra treatment is needed after ESD, it is up to current guidelines.
Exclusion Criteria:
* excessive bleeding and perforation happened during the ESD procedure;
* excessive bleeding and perforation happened during TA injection;
* loss to follow-up or not meet three months follow-up periods;
* allergy to triamcinolone or fibrin glue;
* esophageal recurrence in situ during follow-up period
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06840561
Study Brief:
Protocol Section:
NCT06840561