Comparison of 0.4% Hyaluronic Acid Solution Versus Hydroxyethylamide Solution in Submucosal Endoscopic Resections
Esophageal Neoplasms, Endoscopic Mucosal Resection, Hyaluronic Acid
About this trial
This is an interventional basic science trial for Esophageal Neoplasms focused on measuring Esophageal Neoplasms, Endoscopic Mucosal Resection, Hyaluronic Acid
Eligibility Criteria
Inclusion Criteria: Patients over 18 years of age Superficial esophageal adenocarcinoma or squamous cell carcinoma with indication of ESD after discussion in a multidisciplinary oncological board Signed informed consent form Exclusion Criteria: Residual or recurrent esophageal lesions Ulcerated esophageal lesions Patients with severe cardiovascular, kidney or liver disease History of hypersensitivity to hyaluronic acid Pregnant or lactating women
Sites / Locations
- Instituto do Câncer do Estado de São PauloRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Hydroxyethylamide Group
Hyaluronic acid group (TS-905 Blue Eye)
15 will be from the hydroxyethylamide Group, where the submucosal endoscopic dissection will be performed with submucosal injection of hydroxyethylamide.
15 will be from the Hyaluronic acid group (TS-905 Blue Eye), where the submucosal endoscopic dissection with submucosal injection of hyaluronic acid (TS-905 Blue Eye) will be performed.