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EUS - Guided Balloon-occluded Gastrojejunostomy Bypass

Primary Purpose

Gastric Outlet Obstruction

Status
Completed
Phase
Phase 2
Locations
Hong Kong
Study Type
Interventional
Intervention
EUS-guided gastrojejunstomy
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastric Outlet Obstruction

Eligibility Criteria

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

Inclusion Criteria:

  • Consecutive patients ≥ 18 years old
  • Biopsy and/or cytology confirmed unresectable distal gastric or duodenal or pancreatico-biliary malignancies
  • Suffering from gastric outlet obstruction with a gastric outlet obstruction score of ≤ 1 (appendix 1) 19 Performance status ECOG ≤3 (appendix 2)

Exclusion Criteria:

  • Prior metallic stent placement
  • Severe comorbidities precluding the endoscopic procedure (such as cardiopulmonary disease, sepsis, or a bleeding disorder)
  • Life expectancy of less than 1 month
  • History of gastric surgery
  • Linitus plastic
  • Multiple-level bowel obstruction confirmed on radiographic studies such as small bowel series or abdominal computed tomography
  • Coagulation disorders
  • Pregnancy

Sites / Locations

  • Department of Surgery, Prince of Wales Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

EUS-guided gastrojejunostomy

Arm Description

The procedures would be performed under conscious sedation or monitored anesthesia by a therapeutic gastroscope. The endoscope would be used to reach the site of obstruction. The stricture would be cannulated with a 0.025" or 0.035" guide-wire. The double balloon occluder would then be inserted on guidewire beyond the duodenal-jejunal flexure and the two balloons of the occluder would be inflated. A segment of duodenum/jejunum would then be occluded and saline would be injected. A linear echoendoscope would then be inserted into the stomach to guide insertion of the gastrojejunostomy stent.

Outcomes

Primary Outcome Measures

6 month re-intervention rate
percentage of patients requiring additional endoscopic intervention due to stent dysfunction

Secondary Outcome Measures

technical success
successful placement of a stent across the site of obstruction, as confirmed by endoscopy or fluoroscopy
clinical success
improvement of at least 1 point in the GOOS within 3 days after stent insertion
adverse events rate
graded according to the lexicon of endoscopic adverse
mortality
Death within 30 day of the procedure
Post stenting gastric outlet obstruction scores
Degree of oral intake after stenting
the duration of stent patency
How long the stent remains patent
quality of life assessment scores
EORTC QLQ-C30

Full Information

First Posted
July 19, 2017
Last Updated
November 12, 2021
Sponsor
Chinese University of Hong Kong
Collaborators
Tokyo Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT03223480
Brief Title
EUS - Guided Balloon-occluded Gastrojejunostomy Bypass
Official Title
EUS - Guided Balloon-occluded Gastrojejunostomy Bypass (EPASS) for Unresectable Malignant Gastric Outlet Obstruction.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
August 24, 2018 (Actual)
Primary Completion Date
August 14, 2021 (Actual)
Study Completion Date
August 14, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
Collaborators
Tokyo Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Surgical gastrojejunostomy is the conventional treatment for palliating patients suffering from of inoperable malignant gastric outlet obstruction (GOO). Although, the procedure is associated with a high success and low re-intervention rates, there is a risk of morbidities (10% - 16%) and mortalities (7%). The placement of a pyloro-duodenal self-expandable metallic stent (DSEMS) is an alternative to surgery for the palliating these patients. As compared to surgery, the procedure is associated with shorter hospital stay, reduced morbidities and cost. However, the clinical efficacy of DSEMS is limited by several problems. In uncovered DSEMS, the long-term patency is reduced by tumor ingrowth leading to subsequent re-stenosis. In covered DSEMS, stent migration occurs at a frequency of 14 - 25% and it is a major obstacle to stent patency. As a result, randomized trials comparing uncovered DSEMS and partially or fully covered DSEMS in patients with malignant GOO have reported comparable stent patency between the two types of stents. Recently, the creation of a gastrojejunostomy under EUS (EUS-GJ) guidance using lumen-apposing stents has been described 12-16. The procedure was associated with a technical success rate of around 90% and clinical success of 85% to 100%. The procedure holds the potential to create a gastrojejunostomy without surgery. Furthermore, there is a low risk of tumor ingrowth and stent migration, thus improving the stent patency and reducing the need of re-intervention. However, there is limited data on how EPASS compares to endoscopic stenting. The aim of the current study is thus to compare prospective data on EPASS versus a historical group that received DSEMS.
Detailed Description
In recent years, DSEMSs have provided an attractive alternative to surgery for palliation of malignant gastric outlet obstruction. Several studies have assessed the clinical and technical success rates of DSEMS for malignant gastroduodenal obstruction. Technical success rates of 90% to 100% and clinical success of 80% to 95% was achieved.The procedure was associated with quicker recovery and reduced morbidities as compared to surgical gastrojejunostomies. However, the long-term patency of uncovered DSEMS is limited by the risk of tumor ingrowth that would lead to subsequent re-stenosis of the stents requiring re-intervention. Thus to palliate malignant gastric outlet obstruction, surgical gastrojejunostomy is preferred in patients that are fit for surgery with prolonged life expectancy whilst insertion of DSEMS is preferred in patients that are associated with high-risk for surgery and short life expectancy. Recently, EUS-guided gastrojejunostomies have become possible. In the early description, a common technical problem exists in the series. The target duodenum or jejunum needed for creation of a GJ is collapsed and it is difficult to identify the target organ by EUS from the stomach. Furthermore, the insertion of the stent for creation of the anastomosis may be difficult with a collapsed bowel and this may result in catastrophic outcomes. To overcome this difficulty, our group has published the results of using the double balloon occluder that allows distension of the duodenum in conjunction with the AXIOS stent for creation of a GJ in 20 patients (Endoscopic ultrasonography-guided double-balloon-occluded gastrojejunostomy bypass - EPASS). The technical success rate was 90% (18/20). The median intubation time from the double-balloon tube intubation to stent placement was 25.5 min (range 10-39 min). Post-treatment gastric outlet obstruction scoring system (GOOSS) score improved in all 18 cases in which EPASS was successfully performed. Thus, based on the above results, EUS-GJ may be associated with improved outcomes as compared with conventional procedures for management of malignant GOO. The aim of the current study is to compare the efficacies of EPASS in a prospective multicenter setting versus a historical cohort of uncovered DSEMS for patients suffering from unresectable malignant GOO.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Outlet Obstruction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Model Description
All patients recruited will receive EUS-guided gastrojejunostomy using the double balloon occluder
Masking
None (Open Label)
Masking Description
No masking
Allocation
N/A
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
EUS-guided gastrojejunostomy
Arm Type
Experimental
Arm Description
The procedures would be performed under conscious sedation or monitored anesthesia by a therapeutic gastroscope. The endoscope would be used to reach the site of obstruction. The stricture would be cannulated with a 0.025" or 0.035" guide-wire. The double balloon occluder would then be inserted on guidewire beyond the duodenal-jejunal flexure and the two balloons of the occluder would be inflated. A segment of duodenum/jejunum would then be occluded and saline would be injected. A linear echoendoscope would then be inserted into the stomach to guide insertion of the gastrojejunostomy stent.
Intervention Type
Device
Intervention Name(s)
EUS-guided gastrojejunstomy
Intervention Description
As listed in the arms description
Primary Outcome Measure Information:
Title
6 month re-intervention rate
Description
percentage of patients requiring additional endoscopic intervention due to stent dysfunction
Time Frame
6 months
Secondary Outcome Measure Information:
Title
technical success
Description
successful placement of a stent across the site of obstruction, as confirmed by endoscopy or fluoroscopy
Time Frame
1 day
Title
clinical success
Description
improvement of at least 1 point in the GOOS within 3 days after stent insertion
Time Frame
7 days
Title
adverse events rate
Description
graded according to the lexicon of endoscopic adverse
Time Frame
30 days
Title
mortality
Description
Death within 30 day of the procedure
Time Frame
30 days
Title
Post stenting gastric outlet obstruction scores
Description
Degree of oral intake after stenting
Time Frame
7 days
Title
the duration of stent patency
Description
How long the stent remains patent
Time Frame
6 months
Title
quality of life assessment scores
Description
EORTC QLQ-C30
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Consecutive patients ≥ 18 years old Biopsy and/or cytology confirmed unresectable distal gastric or duodenal or pancreatico-biliary malignancies Suffering from gastric outlet obstruction with a gastric outlet obstruction score of ≤ 1 (appendix 1) 19 Performance status ECOG ≤3 (appendix 2) Exclusion Criteria: Prior metallic stent placement Severe comorbidities precluding the endoscopic procedure (such as cardiopulmonary disease, sepsis, or a bleeding disorder) Life expectancy of less than 1 month History of gastric surgery Linitus plastic Multiple-level bowel obstruction confirmed on radiographic studies such as small bowel series or abdominal computed tomography Coagulation disorders Pregnancy
Facility Information:
Facility Name
Department of Surgery, Prince of Wales Hospital
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

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EUS - Guided Balloon-occluded Gastrojejunostomy Bypass

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