Heart procedure showdown: serpentine twist vs. guidewire for navigating artery curves
NCT ID NCT07707427
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This study compares two methods for guiding catheters through loops and sharp bends in the arm arteries during coronary angiography or angioplasty. The 'Serpentine' technique uses controlled catheter rotation, while the standard method uses a flexible guidewire. Researchers will measure which technique succeeds more often, how long it takes, and safety outcomes in about 200 patients with challenging arm artery anatomy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If one technique proves clearly better, it could become the standard method for handling difficult arm artery anatomy during heart procedures, potentially reducing complications and procedure time.
- What could go wrong
- This is a small, single-center study comparing two established techniques, so the results may not apply broadly. Neither technique is new, so the impact is likely incremental.
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 204 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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Nov 2029
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.
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: * Age ≥18 years * Feasibility of TRA * Indication for coronary angiography * Angiographic documentation of radial or brachial artery loop/tortuosity * Written informed consent Exclusion Criteria: * STEMI - high risk NSTEMI presentation * Hemodynamic instability * Anatomical contraindications (e.g., arteriovenous fistula) * Significant calcification of the radial or brachial artery on angiographic evaluation.
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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 Patras
RECRUITINGPátrai, 26504, Greece
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