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Can a single sildenafil pill boost exercise capacity in pulmonary hypertension?

NCT ID NCT07824674

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 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

Phase 2/3

Runs two stages together: whether the treatment works, then large-scale confirmation.

Participants

About 20 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Dec 2028

An estimate. End dates often move.

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.

Ages

18 to 80 years

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: * 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

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • University Hospital of Zurich, Department of Pulmonology

    RECRUITING

    Zurich, Canton of Zurich, 8091, Switzerland

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