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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03439020
Other study ID # 1709-081-886
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 26, 2018
Est. completion date October 31, 2019

Study information

Verified date November 2019
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date October 31, 2019
Est. primary completion date October 31, 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Plastic stent anchoring
Insert an additional plastic stent to anchor the fully covered self expandable metal stent.
FCSEMS
Insert a fully covered self expandable metal stent (FCSEMS) for malignant biliary stricture

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (2)

Lead Sponsor Collaborator
Seoul National University Hospital Daewoong Pharmaceutical Co. LTD.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Stent migration rate Stent 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
6 months after randomization
Secondary Stent-related adverse events According to lexicon for endoscopic adverse events 6 months after randomization
Secondary Duration of stent patency The period from the insertion of the stent to the point at which stent revision is required 6 months after randomization
Secondary Overall survival Period from stenting to death 6 months after randomization
See also
  Status Clinical Trial Phase
Terminated NCT03530527 - Endoscopic Biliary Drainage in Malignant High Grade Biliary Stricture N/A