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Comparison of 0.4% Hyaluronic Acid Solution Versus Hydroxyethylamide Solution in Submucosal Endoscopic Resections

Primary Purpose

Esophageal Neoplasms, Endoscopic Mucosal Resection, Hyaluronic Acid

Status
Recruiting
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Submucous Endoscopic Dissection with hydroxyethylamide
Submucous Endoscopic Dissection with Hyaluronic acid (TS-905 Blue Eye)
Sponsored by
Instituto do Cancer do Estado de São Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Active Comparator

Active Comparator

Arm Label

Hydroxyethylamide Group

Hyaluronic acid group (TS-905 Blue Eye)

Arm Description

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.

Outcomes

Primary Outcome Measures

Volume of solution
Compare the volume of TS-905 Blue Eye versus the solution of hydroxyethylamide used.

Secondary Outcome Measures

Procedure duration in minutes
Evaluate how the procure lasts using each one of the solutions
Number of additional injections
Evaluate the number of additional injections need to complete the lesion ressection

Full Information

First Posted
September 27, 2023
Last Updated
October 16, 2023
Sponsor
Instituto do Cancer do Estado de São Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT06077981
Brief Title
Comparison of 0.4% Hyaluronic Acid Solution Versus Hydroxyethylamide Solution in Submucosal Endoscopic Resections
Official Title
Comparison of 0.4% Hyaluronic Acid Solution Versus Hydroxyethylamide Solution in Submucosal Endoscopic Resections of Superficial Malignant Esophageal Neoplasms: a Randomized Clinical Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 19, 2023 (Actual)
Primary Completion Date
December 30, 2024 (Anticipated)
Study Completion Date
March 13, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto do Cancer do Estado de São Paulo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a randomized, single-center clinical trial that will compare the efficacy of two substances used in the submucosal cushion formation stage of endoscopic submucosal resections of early esophageal malignant neoplasms. Such substances are hyaluronic acid in the form of TS-905 Blue Eyeₒ and hydroxyethylamide (Voluven®).
Detailed Description
Design of the study: This is a randomized clinical trial in a single center. The lesions will be randomized into three blocks based on the diameter of the largest axis (less than 3 cm, between 3 - 5 cm and greater than 5 cm). Selection of patients: The population studied will be patients with early esophageal neoplasia diagnosed and/or referred for submucosal endoscopic dissection at the São Paulo Cancer Institute (ICESP), University of São Paulo. Evaluation of effectiveness and definitions: Effectiveness will be measured from the degree of usefulness. The degree of utility will be determined from two variables: obtaining or not a complete block resection and additional number of submucosal injections performed during endoscopic dissection. The solution that results in a complete block resection with a number of additional injections of 0 (excellent utility degree) or 1 (good utility degree) will be considered effective.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Neoplasms, Endoscopic Mucosal Resection, Hyaluronic Acid
Keywords
Esophageal Neoplasms, Endoscopic Mucosal Resection, Hyaluronic Acid

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomization shall consist of 30 patients, of which: 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.
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hydroxyethylamide Group
Arm Type
Active Comparator
Arm Description
15 will be from the hydroxyethylamide Group, where the submucosal endoscopic dissection will be performed with submucosal injection of hydroxyethylamide.
Arm Title
Hyaluronic acid group (TS-905 Blue Eye)
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Procedure
Intervention Name(s)
Submucous Endoscopic Dissection with hydroxyethylamide
Intervention Description
The resection will be performed in three stages using hydroxyethylamide : delimitation, incision and dissection. Initially we will inject the hydroxyethylamide and examine the delimitation of the lesion. With Knife itself, using soft or Forced coagulation current, we will circumvent the limits of the lesion with punctual coagulations 5 mm away from it.
Intervention Type
Procedure
Intervention Name(s)
Submucous Endoscopic Dissection with Hyaluronic acid (TS-905 Blue Eye)
Intervention Description
The resection will be performed in three stages using Hyaluronic acid (TS-905 Blue Eye) : delimitation, incision and dissection. Initially we will inject the Blue-Eyed and examine the delimitation of the lesion. With Knife itself, using soft or Forced coagulation current, we will circumvent the limits of the lesion with punctual coagulations 5 mm away from it.
Primary Outcome Measure Information:
Title
Volume of solution
Description
Compare the volume of TS-905 Blue Eye versus the solution of hydroxyethylamide used.
Time Frame
During the procedure
Secondary Outcome Measure Information:
Title
Procedure duration in minutes
Description
Evaluate how the procure lasts using each one of the solutions
Time Frame
During the procedure
Title
Number of additional injections
Description
Evaluate the number of additional injections need to complete the lesion ressection
Time Frame
During the procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fauze Maluf-Filho, PhD
Phone
+5511991919014
Email
fauze.maluf@terra.com.br
First Name & Middle Initial & Last Name or Official Title & Degree
Pierre Pirchner
Phone
+5521986979456
Email
pierrepmm@hotmail.com
Facility Information:
Facility Name
Instituto do Câncer do Estado de São Paulo
City
São Paulo
ZIP/Postal Code
01246-000
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fauze Maluf-Filho, PhD
Phone
+5511991919014
Email
fauze.maluf@terra.com.br

12. IPD Sharing Statement

Learn more about this trial

Comparison of 0.4% Hyaluronic Acid Solution Versus Hydroxyethylamide Solution in Submucosal Endoscopic Resections

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