Can a single sildenafil pill boost exercise capacity in pulmonary hypertension?
NCT ID NCT07824674
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
Researchers are testing whether taking a 20mg sildenafil tablet before exercise helps people with pulmonary arterial hypertension reach a higher maximum workload than a dextrose candy tablet. The trial enrolls about 20 adults with stable PAH who are already on standard treatment. Each participant does exercise tests after each treatment in a cross-over design, so everyone receives both sildenafil and the candy comparison. The main measure is the highest workload reached during a cycling test.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- sildenafil, a drug that widens blood vessels, given as a 20mg tablet
- What this could lead to
- If sildenafil helps, it could offer a simple, on-demand way for people with pulmonary arterial hypertension to get more out of exercise on top of their usual treatment.
- What could go wrong
- This is a small, short-term study of 20 people, so any benefit seen may not hold up in larger or longer trials. Sildenafil can lower blood pressure and cause headaches, flushing, or dizziness, and it is not safe for everyone.
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.
- Phase
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Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- 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.
- Ages
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18 to 80 years
- 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: * Signed Informed consent * Age 18 - 80 years (both sexes) * Pulmonary hypertension (PH) class I (PAH) previously diagnosed according to ESC/ERS 2022/2019 guidelines (mPAP ≥ 20 mmHg, PVR ≥ 2 WU, PAWP ≤ 15 mmHg) during diagnostic right-heart catheterization. * Stable condition, on the same PH-medication for \>4 weeks Exclusion Criteria: * Severe resting hypoxia (PaO2 \<7.3 kPa) * Moderate-to-severe chronic obstructive or restrictive pulmonary disease (FEV1 ≤ 60% predicted, FVC ≤ 60% predicted) * Women with known pregnancy or breast feeding * Other clinically significant concomitant disease states (e.g., severe renal or hepatic disease, unstable cardiovascular disease, etc.) * Concurrent medication with: * Nitric oxide donors (molsidomine, nicrorandil, etc.) * Soluble guanylate cyclase stimulators (riociguat) * Potent CYP3A4 inhibitors (azoles, clarithromycin, protease inhibitors) * History of anterior ischemic optic neuropathy or hereditary retinal disease * Participation in another study with investigational drug with potential influence the study data within the 30 days preceding and during the present study. * Known allergies or hypersensitivity to sildenafil 20mg (Revatio 20mg) or dextrose candy (Dextroenergy) including any of its components
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Hospital of Zurich, Department of Pulmonology
RECRUITINGZurich, Canton of Zurich, 8091, Switzerland
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Other studies related to the condition(s) this trial covers.
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