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Lead apron on patients could shield cardiologists from radiation
NCT ID NCT06931171
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether placing a lead apron on a patient's lower belly and pelvis during heart procedures can reduce radiation exposure for the doctor. The trial involves 500 adults undergoing heart catheterization through the wrist. Researchers will measure the doctor's radiation dose with and without the extra shielding to see if this simple, low-cost method improves safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Patient-applied pelvic lead shielding (lead apron)
- What this could lead to
- If effective, this simple, low-cost method could become a standard practice to protect cardiologists from radiation during common heart procedures.
- What could go wrong
- This is a single-center trial testing a technique that may not reduce radiation as much as hoped, or may be impractical in real-world settings. Results may not apply to all hospitals or procedure types.
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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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 500 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2025
- Expected to finish
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Jun 2026
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 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients undergoing transradial diagnostic coronary angiography or angioplasty. * Adults aged 18 years and older. * Informed consent provided. Exclusion Criteria: * Acute STEMI requiring primary percutaneous coronary intervention (PCI). * Patients undergoing structural heart interventions. * Initially femoral access or crossover to femoral access procedures. * Patients unable to provide informed consent.
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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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First Department of Cardiology, Hippokration General Hospital of Athens
Athens, Attica, 11527, Greece
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First Department of Cardiology, National and Kapodistrian University of Athens, Hippokration General Hospital of Athens
Athens, Attica, 11527, Greece