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Bile Duct StrictureNCT03763214

PTFE Stents for Treatment of Malignant Biliary Strictures

A study testing Stenting with PTFE-coated stent (HILZO) in people with Bile Duct Stricture and Bile Duct Cancer, run by Johannes Vermehren at 1 site in Germany.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

In this randomized trial two two self-expanding metal stents (SEMS) for treatment of malignant biliary strictures are investigated. A newly developed PTFE (Polytetrafluorethylen) (Teflon) stent is tested versus standard covered metal stents. Read more about this study

Who is it for?
Ages 18 to 100 years
What is being tested?
Stenting with PTFE-coated stent (HILZO)
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
64 participants
Where
1 siteGermany
Study dates
1 Mar 2018to Sep 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 100 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Indication for the palliative metal-stent system for malignant stenosis of the distal DHC (bile duct tumors, pancreatic carcinoma, papillary carcinoma, lymphoma, lymph node metastases in the hilum)

Who cannot join

  • Age under 18 years
  • Pregnancy
  • Contraindication to an endoscopic examination
  • Life expectancy under 3 months

Trial locations and contacts

1 site in 1 country.

Mireen Friedrich-Rust, Prof. contact

069-6301-0

mireen.friedrich-rust@kgu.de

Fabian Finkelmeier, Dr. contact

069-6301-0

fabian.finkelmeier@kgu.de

Germany1 site, 1 recruiting
  • Klinikum der J. W. Goethe-Universität

    Frankfurt am Main, 60590

    Mireen Friedrich-Rust, MD, Mireen.Friedrich-Rust@kgu.de

    Recruiting

Other trials in Germany

About this study

Official title: Randomized Comparative Study of Novel PTFE-coated Stents (Hilzo) Versus Standard Silicone-coated Metal Stents (cSEMS) in Distal Malignant DHC Stenosis

In this randomized trial two two self-expanding metal stents (SEMS) for treatment of malignant biliary strictures are investigated.

A newly developed PTFE (Polytetrafluorethylen) (Teflon) stent is tested versus standard covered metal stents. PFTE (Teflon) coating promises improved formability over standard silicone-coated stents, easier removal through the soft surface, and significantly reduced tumor growth through the impermeable surface.

Read the detailed description

ERCP (endoscopic retrograde cholangiopancreatography) is the standard method of treating diseases in the biliopancreatic system and the treatment goal is achieved in a very high proportion of the studies. The ERCP is based on the indirect imaging of the bile ducts by injection of contrast medium, which is visualized in X-ray fluoroscopy. Furthermore, the probing of the bile ducts by means of wire and direct interventions within the bile duct system is possible.

Malignant biliary strictures are caused by various, usually cholangiocellular or pancreatic tumors, whose surgical therapy is complex and often impossible due to advanced disease. Tumors of the papillae, lymphomas and lymph node metastases can also lead to stenosis of the extra hepatic bile ducts.

The outcome of patients with malignant biliary strictures is poor, most are already presenting with advanced disease because early symptoms are rare. In particular, the above-mentioned cholangiocellular carcinomas and pancreatic carcinomas are often resectable only in its early form with high recurrence rates. Furthermore, then only palliative concepts are possible. Various studies have shown that stenting of the biliary tract with drainage of more than 50% of the liver volume improves survival. Metal stents seem to be superior to plastic stents at a slightly higher cholangitis rate. It is therefore considered standard therapy to palliatively treat these patients with more than 3 months of life expectancy using a metal stent.

Two types of stents are currently in use, plastic stents and self-expanding metal stents (SEMS). These in turn are coated (cSEMS) and uncoated (uSEMS). In distal malignant stenosis, both cSEMS and uSEMS can be used, with a higher patency rate for cSEMS and a longer duration of uSEMS retention. The disadvantage of the uSEMS is the tumor ingrowth in the stents and the possibility of re-stenosis. Various studies have shown that metal stents are associated with better bile duct drainage and better retention time compared to plastic stents and have fewer early complications, however, a consensus regarding a survival advantage with metal stents has not yet been substantiated, with the data showing a positive trend. Since metal stents, unlike plastic stents, do not need to be changed, a significant advantage for the patient is the significant reduction in endoscopic examinations and associated hospitalization and complication rates.

PTFE stents are a new development that should significantly reduce tumor ingrowth into the stent and, in particular, allow for a significantly reduced stent migration rate. PFTE (Teflon) coating promises improved formability over standard silicone-coated stents, easier removal through the soft surface, and significantly reduced tumor growth through the impermeable surface. At both ends of the stents are "tulips" which are coated with silicone. This in turn reduces the rate of stent closure by sludge, and in particular, the otherwise very high rate of stent migration should be significantly reduced.

Being tested
Stenting with PTFE-coated stent (HILZO)
Keywords
metal stent, biliary stricture, stenting
Medical subject headings
Bile Duct Neoplasms, Pancreatic Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Stenting with PTFE-coated stent (HILZO)Device

    Placing a metal stent in the biliary tract by duodenoscopy

Study groups in NCT03763214
Study groupRoleWhat they receive
Stenting with PTFE-coated stent (HILZO)ExperimentalThe bile duct is stented with a PTFE-coated stent by duodenoscopy to allow bile duct flow
Receives: Device: Stenting with PTFE-coated stent (HILZO)
Stenting standard silicone coated stentActive comparatorThe bile duct is stented with a standard silicone-coated stent by duodenoscopy to allow bile duct flow
Receives: Device: Stenting with PTFE-coated stent (HILZO)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Stent migration

    Rate of stent migrations

    Measured: 12 month

Secondary outcomes (3)
  1. Stent dysfunction (re-stenosis)

    Stenosis of stent with necessity to do duodenoscopy again

    Measured: 12 month

  2. Number of ERCPs in one year

    Count of the number of duodenoscopy the patients undergo

    Measured: 12 month

  3. Survival rate

    Survival of patientes 12 month after the procedure

    Measured: 12 month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Dec 2018
  2. Study start1 Mar 2018
  3. Primary completionMar 2020 (estimated)
  4. Study completionSep 2020 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized, two arms
Masking
None (open label)
Enrolment
64 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03763214
Sponsor's protocol ID
JWGUHMED1-009
Status last verified
Dec 2018
First submitted
14 May 2018
Last updated
4 Dec 2018
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Stenting with PTFE-coated stent (HILZO) in people with Bile Duct Stricture and Bile Duct Cancer, run by Johannes Vermehren at 1 site in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 4 Dec 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Mireen Friedrich-Rust, Prof. (069-6301-0, mireen.friedrich-rust@kgu.de), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Stent migration (time frame: 12 month). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Dec 2018.

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