New surgery may save more lives from deadly aortic tear
NCT ID NCT06676371
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares two surgical methods for acute Type A aortic dissection, a life-threatening tear in the main artery. One method is the standard hemiarch replacement, and the other is a more complex total arch replacement with a frozen elephant trunk device. Researchers will enroll 150 adults in Hong Kong to see which approach leads to better 30-day survival. The goal is to find the best way to treat this emergency and reduce deaths.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- surgical procedure (total arch replacement with frozen elephant trunk or conventional hemiarch replacement)
- What this could lead to
- If it works, this could establish a better surgical approach for a life-threatening aortic tear, potentially lowering the risk of death within 30 days.
- What could go wrong
- This is an early-stage randomized trial with 150 participants, so results may not apply to all patients. Both surgeries are complex and carry risks like bleeding, stroke, or organ failure.
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 150 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 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 to 80 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: 1. Patient 's age is between 18 and 80 years. 2. Patient is willing and able to give informed consent. 3. Patient has acute type A aortic dissection with entry tear beyond ascending aorta. 4. Patient not in coma/irreversible end organ failure/cardiac massage for resuscitation Exclusion Criteria: 1. There is no identifiable entry tear in the aorta 2. The ascending entry tear extends into aortic arch 3. Patient has entry tear only in ascending aorta 4. Patient with Type B aortic dissection 5. Patient has co-morbidity (i.e. active malignancy (progressive, stable or partial remission)) causing expected survival to be less than 2 years. 6. Patient has any other medical, social, or psychological problems, that in the opinion of the investigator, preclude the patient from participating in this study.
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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
3 sites in 3 countries. 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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Prince of Wales Hospital
Hong Kong, Hong Kong
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Siriraj Hospital - Mahidol University
Bangkok, Thailand
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University Hospital Vienna
Vienna, Austria
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