Pooling patient data could sharpen understanding of Artery-Repair device
NCT ID NCT07704671
First seen Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time
Summary
This study pools individual patient data from multiple previous studies to get a clearer picture of how well the GORE Iliac Branched Endoprosthesis works for treating iliac aneurysms. Researchers will analyze technical success and complication rates in about 1,200 patients. The goal is to produce more reliable evidence than any single study could provide alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Iliac Branched Endoprosthesis (a stent-graft device placed inside the artery to treat an aneurysm)
- What this could lead to
- If successful, this analysis could provide stronger evidence on how well the device works and which patients benefit most, guiding future treatment decisions.
- What could go wrong
- This is a retrospective analysis of existing data, not a new trial. Results depend on the quality and completeness of shared data, and may not reveal new risks or long-term outcomes.
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 1,200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
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
Patients Treated with the GORE® Iliac Branched Endoprosthesis
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: The IPD-IBE is a retrospective analysis of all available individual patient data on treatments of aorto-iliac with the Gore Iliac Branch Endoprosthesis device from previous peer reviewed publications. All authors that confirm to participate and share the data. Exclusion Criteria: Only if authors decline participation and sharing the data.
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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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Rijnstate
RECRUITINGArnhem, Gelderland, 6515 AD, Netherlands
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Other studies related to the condition(s) this trial covers.
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