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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

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT03672019). StuddyBuddy aggregates publicly available trial information.