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One-Stop care: hepatitis c treatment may curb HIV and opioid risks

NCT ID NCT03221309

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

198 people

The number who actually took part.

Started

May 2017

Finished

Feb 2021

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

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

  • HIPS

    Washington D.C., District of Columbia, 20002, United States

  • 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.