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The Efficacy of Plastic Stent Anchoring to Reduce Migration of Metal Stent

The Efficacy of a Fully Covered Self-expandable Metal Stent Anchored by a Plastic Stent for Anti-migration in the Management of Malignant Biliary Strictures: a Prospective Randomized Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03439020
Enrollment
70
Registered
2018-02-20
Start date
2018-02-26
Completion date
2019-10-31
Last updated
2019-11-21

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

Conditions

Malignant Biliary Stricture

Brief summary

The aim of this study is to demonstrate that the group with an additional plastic stent to anchor the fully covered self expandable metal stent (FCSEMS) in patients with malignant biliary stricture has less stent migration than the group with FCSEMS only. The primary outcome is stent migration for 6 months. The secondary outcomes are stent related adverse events, stent patency, and overall survival.

Detailed description

Endoscopic retrograde biliary drainage using a plastic stent for the treatment of malignant biliary stricture has advantages in that it is easy to perform and low cost, but it has a short period of patency. To overcome this drawback, self-expandable metal stents (SEMS) have been developed and are now widely used. But, over time, the SEMS also develop restenosis, due to tumor ingrowth and the tissue hyperplasia caused by the stimulation of the surrounding tissues by the metal thin wire. To overcome these disadvantages, a fully covered self-expandable metal stents (FCSEMS) covered with a polymer coating have been developed and used. However, the FCSEMS showed more stent migration than the uncovered SEMS, which was not superior to the uncovered SEMS in terms of loss of stent function. In order to overcome the limitations of the FCSEMS, small-scale studies have shown that stent migration can be reduced by anchoring the FCSEMS using a plastic stent. To date, there has been no randomized controlled study to determine whether the FCSEMS can be anchored with a plastic stent in patients with malignant biliary stricture to reduce the stent migration. Therefore, the purpose of this study is to evaluate the efficacy of plastic stent anchoring to reduce migration of FCSEMS.

Interventions

PROCEDUREPlastic stent anchoring

Insert an additional plastic stent to anchor the fully covered self expandable metal stent.

PROCEDUREFCSEMS

Insert a fully covered self expandable metal stent (FCSEMS) for malignant biliary stricture

Sponsors

Daewoong Pharmaceutical Co. LTD.
CollaboratorINDUSTRY
Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Malignant biliary stricture requiring biliary drainage through endoscopic procedure

Exclusion criteria

* Previous history of metal stent placement for malignant biliary stricture * Hilar cholangiocarcinoma * Malignant biliary stricture of intrahepatic duct * A recurrence after surgery due to malignant biliary stricture * Life expectancy less than 3 months * Pregnancy * If endoscopy is not possible based on the judgement of the researcher

Design outcomes

Primary

MeasureTime frameDescription
Stent migration rate6 months after randomizationStent migration is classified as proximal or distal migration. Proximal stent migration is defined as any migration of the FCSEMS(Fully covered self expandable metal stent) into the bile duct, preventing its easy removal. Distal stent migration is defined in three ways. The first is when the stent is completely distally migrated without being lodged into the duodenum. The second is when the stent is lodged in the distal bile duct below the stricture. The third case is when the stent is migrated to the distal portion of the stricture and is lodged in the duodenum opposite the papilla

Secondary

MeasureTime frameDescription
Stent-related adverse events6 months after randomizationAccording to lexicon for endoscopic adverse events
Duration of stent patency6 months after randomizationThe period from the insertion of the stent to the point at which stent revision is required
Overall survival6 months after randomizationPeriod from stenting to death

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026