Suspended Overlength Biliary Stents Preventing Duodenobiliary Reflux in Patients With Biliary Stricture
Primary Purpose
Bile Duct Stricture
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
26cm suspended overlength biliary stents
30cm suspended overlength biliary stents
ordinary plastic biliary stents
Sponsored by
About this trial
This is an interventional prevention trial for Bile Duct Stricture
Eligibility Criteria
Inclusion Criteria:
- Unresectable extrahepatic malignant biliary stricture,available for insertion of biliary stents in ERCP to alleviate biliary stricture.
Exclusion Criteria:
- Patients agree with metal biliary stents;
- Patients with biliary stricture need double or multiple stents inserted;
- Patients with previous surgical drainage procedure;
- Patients with resectable biliary occlusion;
- A guidewire could not be passed through the stricture;
- Patients with duodenal obstruction and duodenal endoscopy could not be reached to papillary.;
- Patients with any contraindication to endoscopic procedures or refuse informed consent
Sites / Locations
- Peking University Third HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Other
Arm Label
26cm suspended overlength biliary stents group
30cm suspended overlength biliary stents group
ordinary plastic biliary stents group
Arm Description
Outcomes
Primary Outcome Measures
stent patency and stent occlusion rate
Patients with symptoms of cholangitis and worsening liver function tests suggestive of cholestasis are considered as premature stent occlusion.
Secondary Outcome Measures
mortality of each group
We will compare the mortality of each group after the insertion of biliary stents.
adverse events
Adverse events include complications of post ERCP such as pancreatitis,biliary infection, bleeding, perforation and stent migration etc.
the rate of technical success
Technical success is defined as successful insertion of the stent into the bile duct during ERCP.
Full Information
NCT ID
NCT03310554
First Posted
October 11, 2017
Last Updated
August 10, 2021
Sponsor
Peking University Third Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03310554
Brief Title
Suspended Overlength Biliary Stents Preventing Duodenobiliary Reflux in Patients With Biliary Stricture
Official Title
Prevention of Duodenobiliary Reflux Via Suspended Overlength Biliary Stents in Patients With Biliary Stricture
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 11, 2018 (Actual)
Primary Completion Date
March 10, 2021 (Actual)
Study Completion Date
September 30, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University Third Hospital
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
Endoscopic insertion of plastic or metal stents in bile duct under endoscopic retrograde cholangiopancreatography is a well established treatment of distal malignant biliary obstruction.Biliary stents are widely used to relieve symptoms of malignant biliary stricture.Now, the mainly used biliary stents include plastic and metal stents. The main limitation of long time plastic stents is stents occlusion. Biliary plastic stents are changed every 2 to 3 months due to an expected median patency from 77 to 126 days.Metal stents present a lower risk of recurring biliary occlusion, yet high cost and stents occlusion are eventually inevitable. The mechanism of biliary stents occlusion include biliary sluge of the accumulation of bacteria and duodenal biliary reflux .The anti-reflux barrier of Oddi's sphincter disappears after the insertion of biliary stents and the presure in bile duct lowers the duodenals, which cause the retrograde flow of duodenal material into the biliary ducts. Besides, ordinary biliary plastic stent is short which can also shortens the length of duodenal biliary reflux . Therefore, trying to prevent the duodenal biliary reflux is very important in reducing biliary stents occlusion and it is gradually concerned by clinical researchers. Some studies have showed that plastic stents with antireflux valves can effectively reduce the biliary stent stricture and prolong the stents patency, which means reducing duodenobiliary reflux is surely useful for keeping biliary stent patency.So,we assume to explore an innovatively suspended overlength biliary stents (made from nasobiliary tube with length of 26cm or 30cm) as substitution for ordinary biliary plastic stent to prevent the duodenobiliary reflux by extending the length of duodenal content reflux and avoid the stents shift via suspending in intrahepatic duct. In this study,we will design a randomized controlled trial to compare the patency of different length of suspended overlength biliary stents and ordinary plastic biliary stents in patients with distal malignant biliary obstruction to evaluate the effect and safety of suspended overlength biliary stents for the prevention of duodenobiliary reflux and the effect of different length of the stents.
Detailed Description
Endoscopic insertion of plastic or metal stents in bile duct under endoscopic retrograde cholangiopancreatography is a well established treatment of distal malignant biliary obstruction.Biliary stents are widely used to relieve symptoms of malignant biliary stricture.Now, the mainly used biliary stents include plastic and metal stents. The main limitation of long time plastic stents is stents occlusion. Biliary plastic stents are changed every 2 to 3 months due to an expected median patency from 77 to 126 days.Metal stents present a lower risk of recurring biliary occlusion, yet high cost and stents occlusion are eventually inevitable. The mechanism of biliary stents occlusion include biliary sluge of the accumulation of bacteria and duodenal biliary reflux .The anti-reflux barrier of Oddi's sphincter disappears after the insertion of biliary stents and the presure in bile duct lowers the duodenals, which cause the retrograde flow of duodenal material into the biliary ducts. Besides, ordinary biliary plastic stent is short which can also shortens the length of duodenal biliary reflux . Therefore, trying to prevent the duodenal biliary reflux is very important in reducing biliary stents occlusion and it is gradually concerned by clinical researchers. Some studies have showed that plastic stents with antireflux valves can effectively reduce the biliary stent stricture and prolong the stents patency, which means reducing duodenobiliary reflux is surely useful for keeping biliary stent patency .So,we assume to explore an innovatively suspended overlength biliary stents (made from nasobiliary tube with length of 26cm or 30cm) as substitution for ordinary biliary plastic stent to prevent the duodenobiliary reflux by extending the length of duodenal content reflux and avoid the stents shift via suspending in intrahepatic duct. In this study,we will design a randomized controlled trial to compare the patency of different length of suspended overlength biliary stents and ordinary plastic biliary stents in patients with distal malignant biliary obstruction to evaluate the effect and safety of suspended overlength biliary stents for the prevention of duodenobiliary reflux and the effect of different length of the stents.
The investigators will recruit patients according to admission criteria and exclusion criteria. Eligible patients with distal malignant biliary obstruction will be randomly divided into 26cm suspended overlength biliary stents group (experimental group) 、30cm suspended overlength biliary stents group (experimental group) and ordinary plastic biliary stents group (control group).The test groups will be placed the 26cm or 30cm suspended overlength biliary stents in introhepatic bile duct in ERCP. The control group will be placed ordinary plastic biliary stents in ERCP. The primary endpoint is the duration of stent patency and the rate of stent occlusion.The secondary outcomes include the mortality of each group, adverse events and the rate of technical success.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bile Duct Stricture
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Blinding of endoscopists and patients is impossible.But the endoscopists are not involved in the assessment of outcomes. The outcomes assessments are performed by reviewing physicians blinded to the randomization process. The data manager and statistician are not blinded.
Allocation
Randomized
Enrollment
117 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
26cm suspended overlength biliary stents group
Arm Type
Experimental
Arm Title
30cm suspended overlength biliary stents group
Arm Type
Experimental
Arm Title
ordinary plastic biliary stents group
Arm Type
Other
Intervention Type
Procedure
Intervention Name(s)
26cm suspended overlength biliary stents
Intervention Description
The test group will be placed 26cm suspended overlength biliary stents in introhepatic bile duct in ERCP
Intervention Type
Procedure
Intervention Name(s)
30cm suspended overlength biliary stents
Intervention Description
The test group will be placed 30cm suspended overlength biliary stents in introhepatic bile duct in ERCP
Intervention Type
Procedure
Intervention Name(s)
ordinary plastic biliary stents
Intervention Description
The control group will be placed ordinary plastic biliary stents in bile duct in ERCP
Primary Outcome Measure Information:
Title
stent patency and stent occlusion rate
Description
Patients with symptoms of cholangitis and worsening liver function tests suggestive of cholestasis are considered as premature stent occlusion.
Time Frame
12 months after ERCP
Secondary Outcome Measure Information:
Title
mortality of each group
Description
We will compare the mortality of each group after the insertion of biliary stents.
Time Frame
12 months after ERCP
Title
adverse events
Description
Adverse events include complications of post ERCP such as pancreatitis,biliary infection, bleeding, perforation and stent migration etc.
Time Frame
12 months after ERCP
Title
the rate of technical success
Description
Technical success is defined as successful insertion of the stent into the bile duct during ERCP.
Time Frame
12 months after ERCP
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Unresectable extrahepatic malignant biliary stricture,available for insertion of biliary stents in ERCP to alleviate biliary stricture.
Exclusion Criteria:
Patients agree with metal biliary stents;
Patients with biliary stricture need double or multiple stents inserted;
Patients with previous surgical drainage procedure;
Patients with resectable biliary occlusion;
A guidewire could not be passed through the stricture;
Patients with duodenal obstruction and duodenal endoscopy could not be reached to papillary.;
Patients with any contraindication to endoscopic procedures or refuse informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yonghui Huang, archiater
Phone
13911765322
Email
xuxiao_1028@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yonghui Huang, archiater
Organizational Affiliation
Peking University Third Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking University Third Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yonghui Huang, archiater
Phone
13911765322
Email
xuxiao_1028@126.com
12. IPD Sharing Statement
Plan to Share IPD
No
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Suspended Overlength Biliary Stents Preventing Duodenobiliary Reflux in Patients With Biliary Stricture
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