New MRI study reveals how balloon procedure helps lungs and heart
NCT ID NCT07299227
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at how balloon pulmonary angioplasty (BPA) changes heart and lung function in people with chronic blood clots in the lungs (CTEPH). Researchers will use advanced MRI scans before and after the procedure to measure blood flow and heart performance. The goal is to better understand how BPA improves the body's response to this condition.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- balloon pulmonary angioplasty (a procedure to open blocked lung arteries)
- What this could lead to
- If successful, this could show exactly how balloon angioplasty improves heart and lung function in people with chronic blood clots in the lungs.
- What could go wrong
- This is a small, early observational study (60 people) that measures changes using MRI, not a large trial testing a new treatment. It may not prove long-term benefits or apply to 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.
- 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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Sep 2025
- 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.
Who is studied
All CTEPH patients to undergo BPA
- Ages
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18 to 99 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: * Patient referred to BPA * clinical indication for CMR * capability to give informed consent Exclusion Criteria: * general: non-compliance, \<18 years of age, pregnancy * contraindications for CMR (non-CMR compatible device, chronic kidney disease (eGFR \<30ml/min), allergies (medications)
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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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Kerckhoff-Klinik
RECRUITINGBad Nauheim, Hesse, 61231, Germany
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