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A Fully Covered Irradiation Stent for the Palliation of Malignant Dysphagia

Primary Purpose

Malignant Dysphagia

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Fully covered irradiation stent
Sponsored by
Zhongda Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malignant Dysphagia focused on measuring Malignant dysphagia, Stent, Esophageal neoplasms, Brachytherapy

Eligibility Criteria

20 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Endoscopically and histologically confirmed malignant obstruction of the esophagus or the gastroesophageal junction
  • Progressive dysphagia with a dysphagia score of 2-4
  • Unresectable tumours due to extensive lesions, metastases, or poor medical condition
  • Patients with clear consciousness, cooperation
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0-3
  • Informed consent: authorization and signature

Exclusion Criteria:

  • The superior border of the lesion extending beyond the level of the seventh cervical vertebrae
  • Previous treatment with a stent or surgical resection for the same condition
  • Ulcerative esophageal cancer
  • Esophageal fistula
  • Severe hepatic inadequacy or renal inadequacy

Sites / Locations

  • Zhongda Hospital,Southeast UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Fully covered irradiation stent

Arm Description

A esophageal fully covered segmented irradiation stent loaded with 125I seeds is placed in Patients with malignant dysphagia

Outcomes

Primary Outcome Measures

Recurrent dysphagia
The rate of occurrence of tissue ingrowth or overgrowth, stent migration, and food obstruction.

Secondary Outcome Measures

Dysphagia score
Investigated with the Ogilvie score: 0 for nil, 1 for normal diet avoiding certain foods such as raw apple and steak, 2 for semi-solid diet, 3 for fluids only, and 4 for complete dysphagia, even for liquids.
ECOG performance status
Utilizing ECOG performance status score to assess the functional status.
EORTC QLQ-C30
Utilizing EORTC QLQ-C30 to assess the health-related quility of life.
EORTC QLQ-OG25
Utilizing EORTC QLQ-OG25 to assess the health-related quility of life in patients with cancer of the oesophagus and the oesophago-gastric junction.
Technical success
The rate of adequate placement of the stent in the target position and good passage of contrast medium through the stent into the stomach.
Clinical success
The rate of relief of dysphagia with a decrease of at least one point in the dysphagia score.
Overall survival
Time from initial stenting to the day when the patients died or lost to follow-up.
Stent patency
Time from initial stenting to the day when recurrent dysphagia occured or patients died.
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Adverse events including hemorrhage, perforation, fistula, severe chest pain, and pneumonia.

Full Information

First Posted
June 7, 2017
Last Updated
June 9, 2017
Sponsor
Zhongda Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03186014
Brief Title
A Fully Covered Irradiation Stent for the Palliation of Malignant Dysphagia
Official Title
A Novel Fully Covered Segmented Irradiation Stent Loaded With 125I Seeds for the Palliation of Malignant Dysphagia:a Prospective Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Unknown status
Study Start Date
June 2017 (Anticipated)
Primary Completion Date
October 2018 (Anticipated)
Study Completion Date
October 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zhongda Hospital

4. Oversight

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

5. Study Description

Brief Summary
Dysphagia is the major symptom of patients with malignant esophageal stricture caused predominantly by advanced esophageal cancer. Stent placement is the most commonly used strategies for relieving the dysphagia and a novel irradiation stent loaded with 125I seeds has recently been developed. A multicentre randomized clinical trial demonstrated this irradiation stent can relieve the dysphagia rapidly and prolong the survival of patients with advanced esophageal cancer, but the total stent stenosis rate cannot be ruduced. A novel fully covered segmented retrievable irradiation stent was developed in our institute. The purpose of this study is to evaluate the safety and clinical efficacy of this newly developed irradiation stent in patients with unresectable malignant dysphagia.
Detailed Description
Esophageal cancer is the eighth most common cancer and the sixth leading cause of cancer related mortality worldwide. Most patients have lost chance of surgical resection when they are initially diagnosed, because of late stage cancer or metastasis. Dysphagia is the major symptom of patients with advanced esophageal cancer. The two most commonly used strategies for relieving the dysphagia are stent placement and intraluminal brachytherapy. Stent placement provides a fast improvement of dysphagia, while intraluminal brachytherapy provides a more durable effect on dysphagia. To combine the advantages of the immediate relief of esophageal dysphagia with stent placement and long-term benefit with brachytherapy, a novel irradiation stent loaded with 125I seeds has been developed in the authors' institute. Recently, a multicentre randomized clinical trial demonstrated this novel irradiation stent can relieve the dysphagia rapidly and prolong the survival of patients with advanced esophageal cancer. However, this irradiation stent only provides a slightly longer relief of dysphagia and cannot reduce the total stent stenosis rate, because partly covered stent with uncoated flanges on both ends for anchoring the stent are used. In the past few years, fully covered retrievable stents which allow less tissue overgrowth have been used in patients with longer life expectancy, especially if they are receiving additional palliative therapy like brachytherapy. In order to provide a further longer relief of dysphagia and prevent stent migration caused by tumor regresses with brachytherapy, a fully covered segmented retrievable irradiation stent has been developed. The aim of the current study is to evaluate the clinical efficacy, particularly focus on stent stenosis and stent migration, and safety of this newly developed irradiation stent in patients with unresectable malignant dysphagia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malignant Dysphagia
Keywords
Malignant dysphagia, Stent, Esophageal neoplasms, Brachytherapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
38 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Fully covered irradiation stent
Arm Type
Experimental
Arm Description
A esophageal fully covered segmented irradiation stent loaded with 125I seeds is placed in Patients with malignant dysphagia
Intervention Type
Device
Intervention Name(s)
Fully covered irradiation stent
Intervention Description
A esophageal fully covered segmented irradiation stent loaded with 125I seeds is placed in Patients with malignant dysphagia
Primary Outcome Measure Information:
Title
Recurrent dysphagia
Description
The rate of occurrence of tissue ingrowth or overgrowth, stent migration, and food obstruction.
Time Frame
Participants will be followed till die or lost to follow-up, an expected average of 6 months.
Secondary Outcome Measure Information:
Title
Dysphagia score
Description
Investigated with the Ogilvie score: 0 for nil, 1 for normal diet avoiding certain foods such as raw apple and steak, 2 for semi-solid diet, 3 for fluids only, and 4 for complete dysphagia, even for liquids.
Time Frame
Baseline, post-op 7 days, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months
Title
ECOG performance status
Description
Utilizing ECOG performance status score to assess the functional status.
Time Frame
Baseline, post-op 7 days, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months
Title
EORTC QLQ-C30
Description
Utilizing EORTC QLQ-C30 to assess the health-related quility of life.
Time Frame
Baseline, post-op 7 days, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months
Title
EORTC QLQ-OG25
Description
Utilizing EORTC QLQ-OG25 to assess the health-related quility of life in patients with cancer of the oesophagus and the oesophago-gastric junction.
Time Frame
Baseline, post-op 7 days, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months
Title
Technical success
Description
The rate of adequate placement of the stent in the target position and good passage of contrast medium through the stent into the stomach.
Time Frame
During operation
Title
Clinical success
Description
The rate of relief of dysphagia with a decrease of at least one point in the dysphagia score.
Time Frame
3 days after stent placement
Title
Overall survival
Description
Time from initial stenting to the day when the patients died or lost to follow-up.
Time Frame
Participants will be followed till die or lost to follow-up, an expected average of 6 months.
Title
Stent patency
Description
Time from initial stenting to the day when recurrent dysphagia occured or patients died.
Time Frame
Participants will be followed till die or lost to follow-up, an expected average of 6 months.
Title
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Description
Adverse events including hemorrhage, perforation, fistula, severe chest pain, and pneumonia.
Time Frame
Participants will be followed till die or lost to follow-up, an expected average of 6 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Endoscopically and histologically confirmed malignant obstruction of the esophagus or the gastroesophageal junction Progressive dysphagia with a dysphagia score of 2-4 Unresectable tumours due to extensive lesions, metastases, or poor medical condition Patients with clear consciousness, cooperation Eastern Cooperative Oncology Group (ECOG) performance status score of 0-3 Informed consent: authorization and signature Exclusion Criteria: The superior border of the lesion extending beyond the level of the seventh cervical vertebrae Previous treatment with a stent or surgical resection for the same condition Ulcerative esophageal cancer Esophageal fistula Severe hepatic inadequacy or renal inadequacy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chao Wang, Ph.D
Phone
+86 151 9585 3100
Email
wangchaoseu@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gao-jun Teng, Ph.D,MD
Organizational Affiliation
Zhongda Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zhongda Hospital,Southeast University
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210009
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chao Wang
Email
wangchaoseu@126.com

12. IPD Sharing Statement

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A Fully Covered Irradiation Stent for the Palliation of Malignant Dysphagia

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