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Completed No phase listed Observational Results available

The Patient-Reported Outcomes Project of HCV-TARGET

ClinicalTrials.gov ID: NCT02601820

Public ClinicalTrials.gov record NCT02601820. 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 Sep 24, 2026, 10:49 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

The Patient-Reported Outcomes Project of HCV-TARGET (PROP UP)

Brief summary

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

The PROP UP research study is funded by The Patient Centered Outcomes Research Institute (PCORI). PROP UP is a multi-centered prospective observational study that will evaluate all-oral treatment regimens for chronic hepatitis C viral (HCV) infection regarding several patient-reported outcomes (PROs) such as HCV-associated symptoms, treatment side effects, medication adherence, out of pocket costs, comorbid conditions, and long-term benefits of cure and harms of treatment to compare PROs of different treatment regimens, treatment durations, and patient subgroups. Participants will be recruited from 9 U.S. liver centers. Approximately 1920 patients with HCV infection who are prescribed a regimen containing Sofosbuvir/Ledipasvir(SOF/LED), SOF/Velpatasvir(SOF/VEL), Grazoprevir/Elbasvir(GRZ/ELB), OBV/PTV/r + DSV (PRoD), or daclatasvir/SOF (DAC/SOF) will be recruited and approximately 1600 patients who are approved and begin HCV treatment will be enrolled in the longitudinal study. PRO surveys will be evaluated before, during and after HCV treatment. PROP UP is a collaborative effort between behavioral and biomedical researchers, a patient engagement group and a patient advocacy organization.

Study identification

NCT ID
NCT02601820
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
1,601 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
21 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
Oct 31, 2015
Primary completion
Jun 30, 2018
Completion
Jun 30, 2018
Last update posted
Sep 15, 2019

2015 – 2018

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
University of California at Davis Davis California 95616 —
Yale University New Haven Connecticut 06520 —
University of Florida Gainesville Florida 32611 —
Rush University Chicago Illinois 60612 —
University of Michigan Ann Arbor Michigan 48109 —
St Louis University St Louis Missouri 63104 —
Asheville Gastroenterology Associates Asheville North Carolina 28801 —
University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 —
Wilmington Gastroenterology Associates Wilmington North Carolina 28403 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Virginia Commonwealth University Richmond Virginia 23298 —

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 NCT02601820, 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 Sep 15, 2019 · Synced Sep 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02601820 live on ClinicalTrials.gov.

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