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IRS(Irradiation Stent) vs. CS(Conventional Stent) Insertion in Inoperable Malignant Biliary Obstruction

Study of Stent Insertion Combined With or Without Brachytherapy in Patients With Inoperable Malignant Biliary Obstruction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02001779
Acronym
IRCSMBO
Enrollment
328
Registered
2013-12-05
Start date
2013-10-31
Completion date
2016-09-30
Last updated
2017-02-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignant Biliary Obstruction

Keywords

Malignant biliary obstruction, Obstruction/stricture, Stent, Brachytherapy, Bile duct

Brief summary

Stenting the malignant biliary obstruction is considered to be the preferred palliation modality to relieve pruritus,cholangitis,pain and jaundice in patients without surgical indications of malignant biliary obstruction.An unicentral clinical trial has demonstrated the safety and technical feasibility of an irradiation biliary stent insertion in patients with biliary obstruction caused by adenocarcinomas, such a treatment seems have benefits in relieving jaundice and extending survival when compared to a conventional biliary stent.However,the small sample size,the population distribution of two groups will influence the final results in obtaining a powerful statistical conclusion.Therefore,a multicentric study was designed to prospectively compared the responses to the treatment with this irradiation biliary stent versus the conventional biliary self-expandable stent in patients with inoperable malignant biliary obstruction.

Detailed description

Malignant biliary obstruction is a common condition caused by various carcinomas.The clinical process is usually silent and insidious,only 10-20% patients can be surgically removed once obstructive jaundice occurred.The long-term survival rate after resection remain dismal.Relief of obstructive jaundice plays major role on prognosis in patients without surgical indications.For unresectable patients,stenting the biliary obstruction is considered to be the preferred palliation modality to relieve pruritus,cholangitis,pain and jaundice.Although a number of new techniques for treatment of malignant biliary obstruction have been developed,there have been no significant differences in survival or quality of life comparing surgery bypass versus plastic stent insertion,metal stent insertion versus plastic stents insertion,or covered stent versus uncovered stents insertion in such patients.Our previous unicentric clinical trial has demonstrated the safety and technical feasibility of a biliary intraluminal irradiation stent insertion in patients with biliary obstruction caused by adenocarcinomas, such a treatment seems have benefits in relieving jaundice and extending survival when compared to a conventional biliary stent.However,the small sample size,the population distribution of two groups will influence the final results in obtaining a powerful statistical conclusion in the overall survival and stent patency between two groups.Therefore,a multicentric study was designed to prospectively compared the responses to the treatment with this irradiation biliary stent versus the conventional biliary self-expandable stent in patients with inoperable malignant biliary obstruction.

Interventions

DEVICEBiliary SEMS loaded with 125I seeds

A self-expandable metallic biliary stent loaded with 125 iodine seeds is inserted in patients with inoperable malignant biliary obstruction.

DEVICEConventional biliary SEMS

A self-expandable metallic stent is inserted in patients with inoperable malignant biliary obstruction.

Sponsors

Zhongda Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Clinical,histological or pathological diagnosis of malignant biliary obstruction * Unresectability or refusal to be surgically treated * The Eastern Cooperative Oncology Group(ECOG) scores from 0 to 3 * With symptoms such as jaundice related to biliary obstruction * Willing and able to comply with the study procedures and provide written informed consent to participate in the study * Biliary obstruction of Bismuthe-Corlette,type I and II

Exclusion criteria

* Benign biliary obstruction * The Eastern Cooperative Oncology Group(ECOG) score of 4 * Biliary tract stricture that could not be dilated enough to pass the delivery system * Presence of metallic biliary stent or bile duct surgery * Percutaneous transhepatic cholangiography(PTC) procedure was contraindicated * Active hepatitis * Biliary obstruction of Bismuthe-Corlette,type Ⅲ and Ⅳ * Uncooperative or could not provide authorization and signature

Design outcomes

Primary

MeasureTime frameDescription
PatencyParticipants will be followed till die or lost to follow-up,an expected average of a year.Time from stenting to the day when stricture/obstruction of the stent occured or restricture/reobstruction after recanalization the obstructed stent.

Secondary

MeasureTime frameDescription
Over survivalParticipants will be followed till die or lost to follow-up,an expected average of a year.Time from stenting to the day when the patients died or lost to the follow-up.
Clinical successParticipants will be followed till die or lost to follow-up,an expected average of a year.The rate of relief of the symptoms and signs of the patients.
SafetyParticipants will be followed till die or lost to follow-up,an expected average of a year.Including technique success rate,side effect/complication,radioactive safety.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026