Heart transplant patients get hepatitis c cure hope
NCT ID NCT03886077
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a 12-week course of glecaprevir/pibrentasivir can safely cure hepatitis C in heart transplant patients who got the virus from infected donors. Fifty adults on the transplant waitlist were enrolled, and those who received a hepatitis C-positive heart were treated after infection was confirmed. The main goal was to see if the virus stayed gone 12 weeks after treatment, with a secondary check on heart artery health one year later.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- glecaprevir/pibrentasivir
- What this could lead to
- If successful, this could show that treating hepatitis C after heart transplant is safe and effective, potentially improving outcomes for patients who receive infected donor hearts.
- What could go wrong
- This is a small, early study with only 50 participants and no blinding, so results may not apply to everyone. The long-term effects on heart health are still uncertain.
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
-
50 people
The number who actually took part.
- Started
-
Mar 2019
- Finished
-
Dec 2024
- 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
50 subjects listed for cardiac transplantation will be enrolled. Patients will be educated about this protocol prior to transplant, and informed consent obtained. Enrolled subjects who receive a transplant with a NAT positive HCV infected donor will undergo NAT testing and surveillance post-operatively. In addition, patients who are offered an HCV infectious organ will be "re-consented" at the time of transplantation admission.
- 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.
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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: * Subjects must meet all of the inclusion criteria specified below in order to be eligible for participation in this study 1. Willing and capable of providing written informed consent 2. Age ≥18 years 3. On UNOS list as a candidate for heart transplant Exclusion Criteria: * Subjects who meet any of the following exclusion criteria cannot be enrolled in this study. 1. Individuals under 18 years of age 2. History of advanced liver disease, including active hepatitis B or C, detectable hepatitis B surface Ag, hepatitis B DNA, HCV RNA, or cirrhosis 3. Pregnant individuals 4. HIV antibody positive
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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
-
Sentara Norfolk General Hospital
Norfolk, Virginia, 23507, United States
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