A 30-Minute nailbed scan could reveal how lung treatments work
NCT ID NCT07768644
First seen Aug 17, 2026 · Last updated Aug 18, 2026 · Updated 1 time
Summary
This study explores whether a simple, radiation-free scan of the nailbeds—called nailfold capillaroscopy—can help diagnose and monitor pulmonary hypertension (PH), a condition of high blood pressure in the lungs. Researchers will compare nailbed blood vessel measurements with invasive heart catheter readings in 60 adults with different types of PH. They will also scan patients again after they start pulmonary vasodilator therapy to see if nailbed changes reverse with treatment, potentially offering a less invasive way to track response.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pulmonary vasodilator therapy (including phosphodiesterase inhibitors, prostanoids, endothelin receptor antagonists, and activin ligand traps)
- What this could lead to
- If nailfold scans reliably reflect lung pressures, they could offer a quicker, non-invasive way to help diagnose and monitor pulmonary hypertension, potentially reducing the need for invasive catheter tests.
- What could go wrong
- This is a small, early-stage study. The nailfold changes may not correlate strongly with heart pressures, and any reversibility seen might not translate into a reliable clinical tool.
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
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Aug 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.
Who is studied
Spanning the entire pulmonary population of Scotland
- 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: For inpatient enrolment: * Suspected diagnosis of group 1,3 or 4 pulmonary hypertension undergoing inpatient assessment at nationally designated centre * Age \> 18 years For follow up scanning of those enrolled as an inpatient: * Confirmed diagnosis of pulmonary hypertension assessed at nationally designated centre fulfilling criteria for group 1, 3 or 4 disease * Commencing PH targeted therapy, specifically one or more of: a phosphodiesterase 5 inhibitor (PDE5i), an ET receptor antagonist (ERA), parenteral prostanoid therapy, selexipag, riociguat, sotatercept. For outpatient enrolment * Confirmed diagnosis of pulmonary hypertension assessed at nationally designated centre fulfilling criteria for group 1, 3 or 4 disease * Age \> 18 years * Escalating PH targeted therapy, specifically one or more of: a phosphodiesterase 5 inhibitor (PDE5i), an ET receptor antagonist (ERA), parenteral prostanoid therapy, selexipag, riociguat, sotatercept. Target of \> 25% of patients recruited at diagnosis and to have an SSc-spectrum disorder fulfilling either ACR/EULAR 2013 or VEDOSS (very early diagnosis of SSc) criteria. Target of \> 25% of patients recruited at diagnosis and to have non-SSc group 1 (PAH) diagnosis (as determined by national MDT decision). Exclusion Criteria: * Patients with confirmed group 2 or group 5 pulmonary hypertension * Patients \< 18 years of age * Patients unable to participate in nailbed microscopy (through e.g. amputation, severe contractures or other musculoskeletal issues). * (From follow up) Patients not being commenced on pulmonary vasodilator therapy at the point of diagnosis. * Patients already on maximal PH therapy * Patients lacking capacity to consent to participation * Patients who are non-fluent English speakers, where suitable translation cannot be found within a time frame that makes the study feasible. * Patients with a life expectancy \< 4 months * Patients who have consumed nicotine or caffeine within the last 4 - 6 hours * Patients wearing nail polish / varnish/ extensions that preclude adequate nailbed visualisation.
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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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NHS Golden Jubilee
RECRUITINGClydebank, West Dunbartonshire, G81 4DY, United Kingdom
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