Clinical Trials Directory

Trials / Completed

CompletedNCT04055870

Efficacy, Safety, and Adequacy of EUS-guided Liver Biopsy

Status
Completed
Phase
Study type
Observational
Enrollment
24 (actual)
Sponsor
Methodist Health System · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy, safety, and adequacy of EUS-guided liver biopsy in patients undergoing EUS-guided liver biopsy at Methodist Dallas Medical Center (MDMC).

Detailed description

The purpose of this study is to evaluate the efficacy, safety, and adequacy of EUS-guided liver biopsy in patients undergoing EUS-guided liver biopsy at Methodist Dallas Medical Center (MDMC). This is a clinical quality improvement (CQI) initiative to evaluate outcomes within our institution. The data collected will be used to inform new innovative ways to improve EUS-guided liver biopsy with an ultimate goal of improving the quality of patient care. The clinical outcomes of this patient population have not been previously systematically reviewed in MDMC. Currently, the procedure in not being performed routinely at Methodist Dallas Medical Center (MDMC). However, with new technical and physician expertise, this option is now available at our institution. PI will evaluate the efficacy, safety, and adequacy of EUS-guided liver biopsy in patients requiring histologic examination of their liver at MDMC.

Conditions

Interventions

TypeNameDescription
PROCEDUREEUS-guided liver biopsy at MDMCEndoscopic ultrasound (EUS) guided liver biopsy sampling is emerging as an alternative to the aforementioned approaches that offers several advantages, including decreased sampling variability and procedure-related complications.

Timeline

Start date
2017-08-21
Primary completion
2020-10-30
Completion
2020-10-30
First posted
2019-08-14
Last updated
2021-06-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04055870. Inclusion in this directory is not an endorsement.