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Active Not Recruiting
NCT03672019
A Quality of Life Study in Patients Undergoing Percutaneous Biliary Drainage
Conditions: Malignant Biliary Obstruction
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 118
Sponsor: Memorial Sloan Kettering Cancer Center
Location: Memorial Sloan Kettering Basking Ridge (Consent only) Basking Ridge New Jersey
Summary
The purpose of this study is to compare the participant's health-related quality of life before and after the biliary drainage procedure. The study will also help us learn whether having a drainage catheter or a stent placed during the procedure makes a difference in the participant's quality of life.
Eligibility Criteria
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
Source: ClinicalTrials.gov (NCT03672019). StuddyBuddy aggregates publicly available trial information.