Can bosentan reverse lung artery thickening? small study investigates
NCT ID NCT00595049
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether bosentan (Tracleer) can reduce the thickness of lung artery walls in people with a type of high blood pressure in the lungs (pulmonary arterial hypertension, or PAH). Eleven adults with PAH took bosentan for 6 months. Researchers measured artery wall thickness and how well small blood vessels in the lungs responded to natural chemicals. The goal was to see if the drug could improve artery structure and function.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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11 people
The number who actually took part.
- Started
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May 2006
- Finished
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Jun 2010
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- 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.
Show the full entry requirements Hide 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 : · Men or women \>18 years of age.· * Symptomatic (modified NYHA class III) iPAH or PAH-SSc· * PAH confirmed by right heart catheterization performed within 3 months before enrolment mPAP \> 25 mmHg, PCWP \< 15 mmHg and PVR \> 3 mmHg/l/min. * Women of childbearing potential must have a negative pre-treatment pregnancy test and use a reliable method of contraception during study treatment and for 3 months after study treatment termination. * Bosentan naïve patients Exclusion Criteria : · PAH other than iPAH or PAH-SSc * Significant vasoreactivity during right heart catheterization defined as a fall in mPAP to \< 40 mmHg with a decrease \>= 10 mmHg and with a normal cardiac index (\>= 2.5 l/min.m2)· Severe obstructive lung disease: FEV1/FVC \< 0.5 * Severe restrictive lung disease: TLC \< 0.7 of normal predicted value * Hemoglobin \<75% of the lower limit of the normal range· Systolic blood pressure \< 85 mmHg * Body weight \< 40 kg * Pregnancy or breast-feeding * Moderate to severe hepatic impairment, i.e., Child-Pugh Class B or C. * Baseline aminotransferases, i.e., aspartate aminotransferases (AST) and/or alanine aminotransferases (ALT) \> 3 times the upper limit of the normal (ULN) range. * Treatment for iPAH or PAH-SSc within 1 month before start of study treatment, excluding warfarin and acute administration of vasodilators for vascular reactivity testing during heart catheterization. * Treatment with epoprostenol or other prostacyclin analogs for iPAH or PAH-SSc within 1 month before start of study treatment * Treatment with glibenclamide (glyburide), fluconazole ketoconazole or ritonavir within 1 week before start of study treatment. * Current treatment with cyclosporine A or tacrolimus * Hypersensitivity to bosentan or any of the excipients of its formulation. * Patient who received an investigational drug (such as sildenafil) within 3 months before start of study treatment * Conditions that prevent compliance with the protocol or adherence to therapy.
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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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Royal Prince Alfred Hospital
Camperdown, Australia
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