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Not listed Not applicable Interventional

Digimeds to Optimize Adherence in Patients With Hepatitis C and Increased Risk for Nonadherence

ClinicalTrials.gov ID: NCT03164902

Public ClinicalTrials.gov record NCT03164902. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 4:07 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Evaluation of Wirelessly Observed Therapy to Optimize Adherence in Patients With Hepatitis C and Increased Risk for Nonadherence to Treatment

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study evaluates the ability of digital medicines, Proteus Discover, to promote adherence and thus achieving a cure for hepatitis C in patients at high risk for not adhering to their hepatitis therapy. In this single-arm, prospective study, subjects at high risk for nonadherence will be prescribed hepatitis C therapy that will be co-encapsulated with ingestible sensors (creating the digital medicine) by a pharmacy. Both the subject and the providers will have access to the ingestion adherence.

Study identification

NCT ID
NCT03164902
Recruitment status
Not listed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Proteus Digital Health, Inc.
Industry
Enrollment
253 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 21, 2017 (Actual)
Primary completion
Apr 30, 2019 (Estimated)
Completion
Apr 30, 2019 (Estimated)
Last update posted
Dec 13, 2018

2017 – 2019

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294 —
Zuckerberg San Francisco General Hospital San Francisco California 94110 —
Peak Gastroenterology Associates Colorado Springs Colorado 80907 —
Denver Health Denver Colorado 80204 —
Providence Health System Washington D.C. District of Columbia 20017 —
Orlando Immunology Center Orlando Florida 32803 —
Apex Clinical Research Tampa Florida 33612 —
The Ruth M. Rothstein CORE Center Chicago Illinois 60637 —
Johns Hopkins University Baltimore Maryland 21205 —
The Research Institute Springfield Massachusetts 01105 —
Harper University Hospital Detroit Michigan 48201 —
Henry Ford Health System Detroit Michigan 48202 —
Southwest Care Center Santa Fe New Mexico 87502 —
Duke University Medical Center Durham North Carolina 27710 —
Harborview Medical Center Seattle Washington 98104 —
SSM Health Dean Medical Group Madison Wisconsin 53713 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03164902, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 13, 2018 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03164902 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →