Can a blood pressure drug reverse liver damage in hepatitis c?
NCT ID NCT00148837
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether adding prazosin, a drug usually used for high blood pressure, to standard hepatitis C treatment could reduce liver scarring. 112 adults with chronic hepatitis C (genotype 1 or 4) and severe liver fibrosis took part. Researchers measured changes in liver scarring before and after treatment to see if prazosin made a difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- prazosin
- What this could lead to
- If it works, adding prazosin to standard therapy could help reduce liver scarring in people with hepatitis C and severe fibrosis.
- What could go wrong
- This is a small, early-phase trial with only 112 participants. The benefit may be modest or not confirmed in larger studies, and prazosin can cause side effects like dizziness and low blood pressure.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
112 people
The number who actually took part.
- Start date
-
Sep 2004
- Finished
-
Dec 2008
- Lead sponsor
-
A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- 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: * Chronic viral hepatitis C, genotype 1 or 4 * Fibrosis F3 or F3-F4, assessed by the scoring Metavir system * Initial treatment against HCV Exclusion Criteria: * Psychiatric pathology * Alcool consummation * Pregnancy or plan of pregnancy * Breastfeeding
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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
-
Hopital du haut Leveque
Pessac, 33604, France
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Other studies related to the condition(s) this trial covers.
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