search
Back to results

Water-jet Assisted ESD vs Conventional ESD Technique for Treating Early Gastric Cancer

Primary Purpose

Stomach Neoplasms

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Conventional ESD
Hybridknife ESD
Sponsored by
Shanghai Zhongshan Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stomach Neoplasms focused on measuring Early gastric cancer,, endoscopic submucosal dissection (ESD), water-jet assisted ESD

Eligibility Criteria

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

Inclusion Criteria:

  • adults (≥ 18 years) with confirmed diagnosis of gastric adenoma or early gastric adenocarcinoma
  • differentiated mucosal adenocarinoma without ulcer findings ≤ 60 mm in diameter.
  • Lesions with ulceration ≤ 30 mm in diameter.
  • undifferentiated type of mucosal cancer is ≤ 20 mm.
  • The patient has given written informed consent.

Exclusion Criteria:

  • pregnancy
  • coagulopathy (INR>2.0, platelets < 70/nl)
  • mucosal lesions which did not meet the inclusion criteria
  • evidence of local or distant metastases according to endoscopic ultrasound (EUS) and/or CT scan, EUS (7.5 MHz probe) findings of tumor infiltration into deep layers of the submucosa or muscularis propria. -Patients unfit for deep sedation by use of propofol

Sites / Locations

  • Evangelisches Krankenhaus Düsseldorf

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Conventional ESD

Hybridknife ESD

Arm Description

Conventional ESD: Conventional ESD technique using IT2-Knife, Dual-Knife, Hook-Knife (Olympus Europe, Hamburg, Germany) ERBE VIO 300D (V2.1.4) RF-surgery system (ERBE Elektromedizin GmbH, Tübingen, Germany) Injection of fluid: Syringe

Group 2: Water-jet assisted HybridKnife® ESD technique using HybridKnife® (Erbe Elektromedizin GmbH, Tübingen, Germany) ERBE VIO 300D (V2.1.4) RF-surgery system (ERBE Elektromedizin GmbH, Tübingen, Germany) Injection of fluid: Integrated in HybridKnife® with ERBEJet 2 water-jet surgery system (ERBE Elektromedizin GmbH, Tübingen, Germany)

Outcomes

Primary Outcome Measures

Procedure time
The primary objective of the study is the procedure time of ESD using the conventional ESD technique in comparison to the water-jet assisted HybridKnife®-ESD technique.

Secondary Outcome Measures

en bloc resection rate
Resection of the targeted lesion including coagulation markers in one piece.
histological R0 rate
En-bloc resection and histological confirmation of horizontal and vertical free margins of neoplasia.
Histologically incomplete resection
Tumor infiltrated (R1) or undetermined (RX) margins of the resected specimen.
procedure related morbidity and mortality and complication rate
procedure related morbidity and mortality
complication rate
any complication occurs after procedure within 30 days, such as bleeding or perforation rates

Full Information

First Posted
September 4, 2013
Last Updated
September 11, 2013
Sponsor
Shanghai Zhongshan Hospital
Collaborators
Evangelisches Krankenhaus Düsseldorf
search

1. Study Identification

Unique Protocol Identification Number
NCT01943253
Brief Title
Water-jet Assisted ESD vs Conventional ESD Technique for Treating Early Gastric Cancer
Official Title
Water-jet Assisted Endoscopic Submucosal Dissection (ESD) in Comparison to Conventional ESD Technique for Treatment of Early Gastric Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
October 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Zhongshan Hospital
Collaborators
Evangelisches Krankenhaus Düsseldorf

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Introduction The aim of the study is to evaluate the efficacy and safety of ESD by use of a new water-jet assisted ESD system using the HybridKnife® in patients with early gastric neoplastic lesions in comparison to the conventional ESD established in Japan. The water-assisted ESD technology allows pressure controlled injection of fluids through the tip of a recently developed HybridKnife®. Submucosal injection, circumferential cutting and dissection of lesions as well as coagulation of bleeding can be performed with the same device without need for changing the instrument. These options should accelerate the procedure and may increase its safety and efficacy. Hypothesis The water-jet assisted ESD technique using the HybridKnife® bears the advantage of less instrument changes due to the combination of high-frequency cutting and water-jet application in one single instrument. This should lead to a simplified ESD procedure, shorter learn-ing curve and especially to a shorter procedure time. The water-jet assisted ESD technique should be shorter than the conventional ESD techniques using IT2-, Dual- and Hook-Knifes at least with the same safety and effectiveness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stomach Neoplasms
Keywords
Early gastric cancer,, endoscopic submucosal dissection (ESD), water-jet assisted ESD

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
117 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Conventional ESD
Arm Type
Active Comparator
Arm Description
Conventional ESD: Conventional ESD technique using IT2-Knife, Dual-Knife, Hook-Knife (Olympus Europe, Hamburg, Germany) ERBE VIO 300D (V2.1.4) RF-surgery system (ERBE Elektromedizin GmbH, Tübingen, Germany) Injection of fluid: Syringe
Arm Title
Hybridknife ESD
Arm Type
Active Comparator
Arm Description
Group 2: Water-jet assisted HybridKnife® ESD technique using HybridKnife® (Erbe Elektromedizin GmbH, Tübingen, Germany) ERBE VIO 300D (V2.1.4) RF-surgery system (ERBE Elektromedizin GmbH, Tübingen, Germany) Injection of fluid: Integrated in HybridKnife® with ERBEJet 2 water-jet surgery system (ERBE Elektromedizin GmbH, Tübingen, Germany)
Intervention Type
Device
Intervention Name(s)
Conventional ESD
Intervention Description
Conventional ESD: Conventional ESD technique using IT2-Knife, Dual-Knife, Hook-Knife (Olympus Europe, Hamburg, Germany; Olympus Japan) ERBE VIO 300D (V2.1.4) RF-surgery system (ERBE Elektromedizin GmbH, Tübingen, Germany) Injection of fluid: Syringe
Intervention Type
Device
Intervention Name(s)
Hybridknife ESD
Other Intervention Name(s)
Water-jet assisted HybridKnife® ESD
Intervention Description
Group 2: Water-jet assisted HybridKnife® ESD technique using HybridKnife® (Erbe Elektromedizin GmbH, Tübingen, Germany) ERBE VIO 300D (V2.1.4) RF-surgery system (ERBE Elektromedizin GmbH, Tübingen, Germany) Injection of fluid: Integrated in HybridKnife® with ERBEJet 2 water-jet surgery system (ERBE Elektromedizin GmbH, Tübingen, Germany)
Primary Outcome Measure Information:
Title
Procedure time
Description
The primary objective of the study is the procedure time of ESD using the conventional ESD technique in comparison to the water-jet assisted HybridKnife®-ESD technique.
Time Frame
during procedure
Secondary Outcome Measure Information:
Title
en bloc resection rate
Description
Resection of the targeted lesion including coagulation markers in one piece.
Time Frame
in procedure
Title
histological R0 rate
Description
En-bloc resection and histological confirmation of horizontal and vertical free margins of neoplasia.
Time Frame
7 days after procedure
Title
Histologically incomplete resection
Description
Tumor infiltrated (R1) or undetermined (RX) margins of the resected specimen.
Time Frame
7 days after procedure
Title
procedure related morbidity and mortality and complication rate
Description
procedure related morbidity and mortality
Time Frame
30 days after procedure
Title
complication rate
Description
any complication occurs after procedure within 30 days, such as bleeding or perforation rates
Time Frame
30 days after procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adults (≥ 18 years) with confirmed diagnosis of gastric adenoma or early gastric adenocarcinoma differentiated mucosal adenocarinoma without ulcer findings ≤ 60 mm in diameter. Lesions with ulceration ≤ 30 mm in diameter. undifferentiated type of mucosal cancer is ≤ 20 mm. The patient has given written informed consent. Exclusion Criteria: pregnancy coagulopathy (INR>2.0, platelets < 70/nl) mucosal lesions which did not meet the inclusion criteria evidence of local or distant metastases according to endoscopic ultrasound (EUS) and/or CT scan, EUS (7.5 MHz probe) findings of tumor infiltration into deep layers of the submucosa or muscularis propria. -Patients unfit for deep sedation by use of propofol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Horst Neuhaus
Organizational Affiliation
Evangelisches Krankenhaus Düsseldorf
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Pinghong Zhou
Organizational Affiliation
Endoscopy Center, Zhongshan Hospital, Fudan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Evangelisches Krankenhaus Düsseldorf
City
Düsseldorf
Country
Germany

12. IPD Sharing Statement

Learn more about this trial

Water-jet Assisted ESD vs Conventional ESD Technique for Treating Early Gastric Cancer

We'll reach out to this number within 24 hrs