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Short-term Stenting Versus Balloon Dilatation for Dominant Strictures in Primary Sclerosing Cholangitis

Primary Purpose

Primary Sclerosing Cholangitis

Status
Unknown status
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
plastic endoprosthesis
balloon dilatation
Sponsored by
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Primary Sclerosing Cholangitis focused on measuring psc, dominant stricture

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • PSC ascertained with MRCP, ERCP, PTC and/or liver biopsy or
  • PSC highly suspected and to be confirmed with present ERCP
  • Age between 18-75 years
  • Total bilirubin > 3x ULN or rsie in alkaline phosphatase or bilirubin > 50% together with increase in cholestatic complaints

Exclusion Criteria:

  • Prior stenting or balloon-dilatation within last 6 months
  • Clinical signs serious suppurative cholangitis reflected by either fever > 39.0 °C, tachycardia, leukocytosis and elevated CRP, or fever > 38,5 C together with purulent bile found during ERCP.
  • Change of ursodeoxycholic acid therapy shorter than two months ago.
  • Inability to give written informed consent
  • Signs of biliary cirrhosis Child-Pugh B or C
  • Estimated transplant-free survival shorter than 2 years as calculated by a Mayo score < 2
  • Serious suspicion of cholangiocarcinoma, reflected by an imaging study suggestive of metastasis, MRCP with mass lesion with contrast enhancement, rise in CA19.9 of > 63 U/ml with an absolute value > 130 U/ml 14 .
  • Signs of current malignancy other than basocellular skin carcinoma.
  • Inability to give informed consent.
  • Life expectancy < 24 months.
  • Use of antibiotics in previous 4 weeks.

Sites / Locations

  • UZLeuvenRecruiting
  • Academic Medical CenterRecruiting
  • RikshospitaletRecruiting
  • Karolinska InstituteRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

short-term stenting

balloon dilatation

Arm Description

one 10 Fr Plastic endoprosthesis or 2 7 Fr plastic endoprosthesis inserted through dominant stricture(s), to be extracted after 1-2 weeks

4 cm 6 mm biliary dilatation balloon to be inflated for 2 minutes in dominant stricture(s)

Outcomes

Primary Outcome Measures

recurrence-free interval of the primary dominant stricture

Secondary Outcome Measures

number of patients with adverse events in both groups
adverse events within first 3 months after the intervention

Full Information

First Posted
April 25, 2011
Last Updated
July 5, 2012
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
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1. Study Identification

Unique Protocol Identification Number
NCT01398917
Brief Title
Short-term Stenting Versus Balloon Dilatation for Dominant Strictures in Primary Sclerosing Cholangitis
Official Title
Multicenter Randomized Trial Comparing Short-term Stenting Versus Balloon Dilatation for Dominant Strictures in Primary Sclerosing Cholangitis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Unknown status
Study Start Date
May 2011 (undefined)
Primary Completion Date
May 2015 (Anticipated)
Study Completion Date
May 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Primary sclerosing cholangitis (PSC) is a chronic inflammatory disease of the biliary tract of unknown origin. Around 50% of patients develop during their disease course narrowing of the main bile duct with corresponding increase in symptoms such as itching, jaundice and abdominal pain. These narrowings can be treated by balloon dilatation or temporary insertion of a plastic endoprosthesis. However, it is not known which of these two therapeutic modalities is best. This study aims to compare both techniques in order to determine which is best in terms of postponing recurrence of the narrowing, safety and costs.
Detailed Description
Rationale: Primary sclerosing cholangitis is a chronic progressive fibro-obliterative disease of the biliary tree leading to biliary cirrhosis. During its course, dominant strictures occur in approximately 50% of patients. These can be accompanied by lead worsening of symptoms and jaundice and are an indication for endoscopic treatment. The best form of treatment, either balloon dilatation or short-term stent placement, has never been formally investigated. Objective: Primary: To compare the efficacy of single session balloon dilatation versus short-term stent placement in non-advanced PSC patients with regard to re-intervention free recurrence rate at two years. Secondary: To compare the short term efficacy of single balloon dilatation versus short-term stenting with regard to improvement of cholestatic symptoms, biochemical cholestasis, and quality of life in non-endstage PSC patients at three months; to compare the safety of single balloon dilatation session versus short-term stenting in non advanced PSC patients during two years. Study design: This is a multicenter, open-label, randomized intervention study. Study population: Non-advanced primary sclerosing cholangitis subjects with progression of cholestatic complaints from the outpatient population of the seven participating centres. Main study parameters/endpoints: Difference in re-intervention free survival time between both groups at two years. Change in semi-quantitative scoring of cholestatic symptoms (pruritus, right upper quadrant pain, fatigue) from baseline at three months. Change in total bilirubin, alkaline phosphatase, and yGT from baseline at 3 months. Safety: adverse events, clinical laboratory values, vital signs. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Currently, both interventions belong to standard patient care armamentarium. Burden for the patient exists in slightly more regular follow-up visits for two years (three-monthly instead of every 3-4 months) to their treating centre. ERCP is associated with a low mortality (<0.5 %) and acceptable morbidity (overall 5%). Most dreaded complications are severe post-ERCP pancreatitis (<2%) and suppurative cholangitis (<2%). From the available retrospective literature data the incidence of these complications does not seem to differ between the two treatment modalities. ERCP will only be performed when there is a clearcut clinical indication anyway.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Sclerosing Cholangitis
Keywords
psc, dominant stricture

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
short-term stenting
Arm Type
Active Comparator
Arm Description
one 10 Fr Plastic endoprosthesis or 2 7 Fr plastic endoprosthesis inserted through dominant stricture(s), to be extracted after 1-2 weeks
Arm Title
balloon dilatation
Arm Type
Active Comparator
Arm Description
4 cm 6 mm biliary dilatation balloon to be inflated for 2 minutes in dominant stricture(s)
Intervention Type
Procedure
Intervention Name(s)
plastic endoprosthesis
Other Intervention Name(s)
plastic stent
Intervention Description
one 10 Fr Plastic endoprosthesis or 2 7 Fr plastic endoprosthesis inserted through dominant stricture(s), to be extracted after 1-2 weeks
Intervention Type
Procedure
Intervention Name(s)
balloon dilatation
Other Intervention Name(s)
biliary dilatation balloon
Intervention Description
4 cm 6 mm biliary dilatation balloon to be inflated for 2 minutes in dominant stricture(s)
Primary Outcome Measure Information:
Title
recurrence-free interval of the primary dominant stricture
Time Frame
24 months
Secondary Outcome Measure Information:
Title
number of patients with adverse events in both groups
Description
adverse events within first 3 months after the intervention
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: PSC ascertained with MRCP, ERCP, PTC and/or liver biopsy or PSC highly suspected and to be confirmed with present ERCP Age between 18-75 years Total bilirubin > 3x ULN or rsie in alkaline phosphatase or bilirubin > 50% together with increase in cholestatic complaints Exclusion Criteria: Prior stenting or balloon-dilatation within last 6 months Clinical signs serious suppurative cholangitis reflected by either fever > 39.0 °C, tachycardia, leukocytosis and elevated CRP, or fever > 38,5 C together with purulent bile found during ERCP. Change of ursodeoxycholic acid therapy shorter than two months ago. Inability to give written informed consent Signs of biliary cirrhosis Child-Pugh B or C Estimated transplant-free survival shorter than 2 years as calculated by a Mayo score < 2 Serious suspicion of cholangiocarcinoma, reflected by an imaging study suggestive of metastasis, MRCP with mass lesion with contrast enhancement, rise in CA19.9 of > 63 U/ml with an absolute value > 130 U/ml 14 . Signs of current malignancy other than basocellular skin carcinoma. Inability to give informed consent. Life expectancy < 24 months. Use of antibiotics in previous 4 weeks.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cyriel Y Ponsioen, Dr.
Phone
+31 20 5666012
Email
c.y.ponsioen@amc.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Florien M Toxopeus, Drs.
Phone
+31 20 5663005
Email
f.m.toxopeus@amc.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cyriel Y Ponsioen, dr.
Organizational Affiliation
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Official's Role
Principal Investigator
Facility Information:
Facility Name
UZLeuven
City
Leuven
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Werner van Steenbergen, Prof
Phone
+3216340749
Email
werner.vansteenbergen@uzleuven.be
First Name & Middle Initial & Last Name & Degree
Natalie van den Ende, BsC
Phone
+32 16340749
Email
natalie.vandenende@uzleuven.be
Facility Name
Academic Medical Center
City
Amsterdam
ZIP/Postal Code
1100 DE
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cyriel Ponsioen, MD PhD
Phone
+31 20 5666012
Email
c.y.ponsioen@amc.uva.nl
First Name & Middle Initial & Last Name & Degree
Florien Toxopeus, MsC
Phone
+31 20 5669111
Email
f.m.toxopeus@amc.uva.nl
First Name & Middle Initial & Last Name & Degree
Cyriel Ponsioen, MD PhD
Facility Name
Rikshospitalet
City
Oslo
ZIP/Postal Code
N-0027
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lars Aabakken, Prof.
Phone
+47 23072387
Email
lars.aabakken@medisin.uio.no
First Name & Middle Initial & Last Name & Degree
Vemund Paulsen, MD
Phone
+47 23070000
Email
vemund.paulsen@meisin.uio.no
First Name & Middle Initial & Last Name & Degree
Lars Aabakken, MD PhD
Facility Name
Karolinska Institute
City
Stockholm
ZIP/Postal Code
141 86
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Annika Bergquist, prof
Phone
+46 8 58582465
Email
annika.bergquist@ki.se
First Name & Middle Initial & Last Name & Degree
Urban Arnelo, dr
Phone
+46 8 58582465
Email
urban.arnelo@ki.se
First Name & Middle Initial & Last Name & Degree
Annika Bergquist, MD PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
29803836
Citation
Ponsioen CY, Arnelo U, Bergquist A, Rauws EA, Paulsen V, Cantu P, Parzanese I, De Vries EM, van Munster KN, Said K, Chazouilleres O, Desaint B, Kemgang A, Farkkila M, Van der Merwe S, Van Steenbergen W, Marschall HU, Stotzer PO, Thorburn D, Pereira SP, Aabakken L. No Superiority of Stents vs Balloon Dilatation for Dominant Strictures in Patients With Primary Sclerosing Cholangitis. Gastroenterology. 2018 Sep;155(3):752-759.e5. doi: 10.1053/j.gastro.2018.05.034. Epub 2018 May 24.
Results Reference
derived

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Short-term Stenting Versus Balloon Dilatation for Dominant Strictures in Primary Sclerosing Cholangitis

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