One-Stop care: hepatitis c treatment may curb HIV and opioid risks
NCT ID NCT03221309
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new way to care for people who inject drugs and have hepatitis C. Along with standard hepatitis C treatment, participants were offered HIV prevention medication and buprenorphine for opioid use disorder. The goal was to see if this combined approach could cure hepatitis C, reduce HIV risk, and support recovery. The study enrolled 198 adults with ongoing injection drug use.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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198 people
The number who actually took part.
- Started
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May 2017
- Finished
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Feb 2021
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adults infected with HCV and have on-going misuse with opioids
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 18 years old 2. Able and willing to sign informed consent 3. Chronically infected with HCV, defined as any individual with documentation of positive HCV antibody and positive HCV RNA test (HCV RNA of 2,000 IU/mL or greater). 4. Willing to have samples stored for future use 5. Ongoing injection drug use, defined as self-report of either: 1. Phase 1 (first 100 enrolled participants) Injection non-prescription drug use within three months of screening visit or 2. Phase 2 (enrolled participants 101-200) Use of non-prescription opioids within twelve months of screening visit Exclusion Criteria: 1. Decompensated liver disease (Childs Pugh B or C) 2. Unable to comply with research study visits 3. Poor venous access not allowing screening laboratory collection 4. Have any condition that the investigator considers a contraindication to study participation 5. Pregnant or breastfeeding woman
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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HIPS
Washington D.C., District of Columbia, 20002, United States
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University of Maryland Drug Treatment Center
Batlimore, Maryland, 21223, United States
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Other studies related to the condition(s) this trial covers.
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