Draining the bile duct: does it improve daily life for cancer patients?
NCT ID NCT03672019
First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time
Summary
This study tracks quality of life in 118 people with cancer who have a blocked bile duct and undergo a drainage procedure. Participants fill out a questionnaire before the procedure and again at 4 weeks, 12 weeks, and 6 months after. The goal is to see whether a drainage catheter or a stent leads to better day-to-day well-being.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors understand which drainage method (catheter or stent) better preserves quality of life for people with cancer-related bile duct blockages.
- What could go wrong
- This is an observational study, not a treatment trial. It measures patient-reported outcomes but does not test a new therapy, so it cannot directly improve survival or cure the underlying cancer.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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118 people
The number who actually took part.
- Started
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Sep 2018
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Potential research subjects will be identified in the interventional radiology clinic or while admitted based on a request for a biliary drainage procedure from their primary oncologist or surgeon at MSK.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with known malignancy presenting for treatment of biliary obstruction * Undergoing initial Interventional Radiology PBD procedure * Fluent in English to enable instrument completion * At least18 years of age * Must be physically and mentally capable of completing instruments * Must be able to comprehend and execute informed consent Exclusion Criteria: * Patients will be excluded if: * Indication for drainage is acute, symptomatic cholangitis requiring an emergent procedure * Previous PBD procedure * Presence of an indwelling biliary stent * Medical or psychiatric condition that, in the judgment of the consenting professional, prevents appropriate comprehension and execution of either the informed consent or the study instruments
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Memorial Sloan Kettering Basking Ridge (Consent only)
Basking Ridge, New Jersey, 07920, United States
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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Memorial Sloan Kettering Commack (Consent only)
Commack, New York, 11725, United States
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Memorial Sloan Kettering Monmouth (Consent only)
Middletown, New Jersey, 07748, United States
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Memorial Sloan Kettering Westchester (Consent only)
Harrison, New York, 10604, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- New study tests safer bile duct drainage for cancer patients
- New study compares two drainage techniques to ease jaundice in advanced cancer patients
- Which stent is best for unblocking bile ducts in cancer patients?