The Effect of Aspirin on Patency of Metal Stent in Malignant Distal Bile Duct Obstruction

Sponsor
Woo Hyun Paik (Other)
Overall Status
Terminated
CT.gov ID
NCT03279809
Collaborator
(none)
52
1
2
34.8
1.5

Study Details

Study Description

Brief Summary

The aim of this study is to determine whether administration of aspirin can help maintain the patency of metallic stents for distal malignant common bile duct obstruction. Metal stents are mainly used for malignant biliary obstruction if the surgical treatment is not considered and its maintenance period has been reported to be about 8 months. This study will be prospectively conducted as a randomized controlled study with aspirin treated patients who received metal stents in patients over 20 years who were confirmed malignant distal biliary obstruction. The primary endpoint is the incidence of stent dysfunction in both groups for 6 months after the procedure. The secondary endpoints included duration of metallic stent patency, incidence of further procedures, and adverse events related with aspirin.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Background -Endoscopic drainage is the first choice for bile drainage in patients with malignant distal biliary obstruction. Metal stents are mainly used for malignant biliary obstruction if the surgical treatment is not considered. Metal stents have proven superior in many clinical aspects over plastic stents. Nonetheless, the maintenance period of the metallic stent patency has been reported to be around 8 months, and it is often necessary to undergo further procedure due to dysfunction of stents. Recently, it has been reported that the duration of the metallic stent patency in patients with aspirin is prolonged. Since the previous study was a retrospective study, this study will be prospectively conducted as a randomized controlled study with aspirin treated patients who received metal stents in patients over 20 years who were confirmed malignant distal biliary obstruction. The incidence of stent dysfunction in both groups for 6 months after the procedure will be compared. Stent dysfunction is defined as any case which further procedure is required due to jaundice or cholangitis after stent insertion.

Study aim

-The aim of this study is to determine whether administration of aspirin can help maintain the patency of metallic stents for distal malignant common bile duct obstruction.

Data analysis

  • Blinding will remain in place until the statistician codes the statistical analyses of the primary and secondary outcomes. The statistical analyses will be done using the full analysis set according to the intention-to-treat principle, meaning all the randomized patients will be analyzed in their allocated groups regardless of any protocol violations or early treatment discontinuations. The outcomes through a per-protocol analysis set that will consider only the subjects who followed the protocol effectively will be analyzed.

  • The rate of stent dysfunction will be compared using Pearson's chi-squared test with Fisher's exact test and calculated the odds ratio of the event. The secondary outcomes (i.e., the duration of stent patency, the rate of reintervention, and the adverse events related to aspirin administration) will be analyzed using Pearson's chi-squared test with Fisher's exact test, Student's t-test, and Kaplan-Meier curves stratified by drug and the hazard ratios between two groups using the Cox proportional hazards. The further affecting factors for stent dysfunction will be assessed by univariable and multivariable logistic regression analysis.

  • In the initial plan, it was decided not to perform interim analysis, but it was confirmed that more adverse events occurred than expected in the process of conducting the study. Therefore, the interim analysis was performed with the data up to May 2020, and determine whether to continue the study by measuring the benefits and losses obtained from aspirin.

Study Design

Study Type:
Interventional
Actual Enrollment :
52 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:
Double blind
Primary Purpose:
Treatment
Official Title:
The Effect of Aspirin on Patency of Metal Stent in Malignant Distal Bile Duct Obstruction
Actual Study Start Date :
Oct 12, 2017
Actual Primary Completion Date :
Sep 5, 2020
Actual Study Completion Date :
Sep 5, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Intervention : aspirin medication Case with aspirin medication for 6 months after stenting

Drug: Aspirin
Aspirin medication (100mg daily) after biliary stent insertion for malignant obstruction
Other Names:
  • Aspirin 100 mg
  • Placebo Comparator: Control

    Control : placebo medication Case with placebo medication for 6 months after stenting

    Drug: Placebo
    Case with placebo medication for 6 months after stenting
    Other Names:
  • Placebo drug of aspirin
  • Outcome Measures

    Primary Outcome Measures

    1. Incidence of stent dysfunction [6 months after biliary metalic stent]

      Dysfunction after 6 months from stenting

    Secondary Outcome Measures

    1. Duration of metalic stent patency [6 months after biliary metalic stent]

      Duration from insertion time to metallic stent dysfunction time

    2. Incidence of further procedures [6 months after biliary metalic stent]

      Incidence of further procedures needed for biliary drainage

    3. Adverse events related with aspirin [6 months after biliary metalic stent]

      Adverse events which clearly related with aspirin admistration including bleeding event

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Malignant distal bile duct obstruction

    • Over 20 years old

    • Techinical success of endoscopic retrograde biliary drainage with metalic stent

    Exclusion Criteria:
    • Patient's denial

    • Previous Aspirin use

    • Aspirin allergy

    • Contraindication for aspirin

    • Life expectancy < 6mo

    • Gastroduodenal ulcer

    • History of substance abuse

    • Participation in a clinical trial within the past 30 days

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Seoul National University Hospital Seoul Jongno-gu Korea, Republic of 110-744

    Sponsors and Collaborators

    • Woo Hyun Paik

    Investigators

    • Study Chair: Woo Hyun Paik, MD, PhD, Seoul National University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Woo Hyun Paik, Professor, Seoul National University Hospital
    ClinicalTrials.gov Identifier:
    NCT03279809
    Other Study ID Numbers:
    • H-1707-161-874
    First Posted:
    Sep 12, 2017
    Last Update Posted:
    Mar 17, 2021
    Last Verified:
    Mar 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 17, 2021