DBS TaT in Peer-assisted Telemedicine for Hepatitis C - Trial NCT06409169
Access comprehensive clinical trial information for NCT06409169 through Pure Global AI's free database. This phase not specified trial is sponsored by Oregon Health and Science University and is currently Not yet recruiting. The study focuses on Hepatitis C. Target enrollment is 183 participants.
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Study Focus
Sponsor & Location
Oregon Health and Science University
Timeline & Enrollment
N/A
May 01, 2024
May 01, 2026
Primary Outcome
HCV Treatment Initiation
Summary
The purpose of this study is to compare the rate of treatment initiation achieved by
 peer-assisted telemedicine contingent on phlebotomy (usual care) versus that achieved with a
 new protocol, called Dried Blood Spot Test and Treat (DBS TaT). DBS TaT includes DBS testing
 to diagnose hepatitis C (HCV), utilizes a novel clinical decision aid that identifies
 patients who are low risk for hepatic (liver) fibrosis, and directs those patients to HCV
 treatment initiation prior to routine hepatic fibrosis assessment.
 
 The investigators hypothesize that DBS TaT will increase the rate of HCV treatment initiation
 compared to peer-assisted telemedicine contingent on phlebotomy (usual care).
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06409169
Non-Device Trial