Massive saudi study to track heart bypass success rates
NCT ID NCT07316777
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will create a national registry to collect data on 3,000 adults undergoing coronary artery bypass graft (CABG) surgery in Saudi Arabia. The goal is to track complications, recovery, and quality of life for one year after surgery. This information will help hospitals improve care and set national standards for heart surgery.
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 3,000 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 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
Adult patients (≥18 years) undergoing coronary artery bypass grafting (CABG) at participating cardiac surgery centers in Saudi Arabia. The population includes individuals receiving isolated CABG or CABG with concomitant procedures, performed electively, urgently, or emergently, using on-pump, off-pump, minimally invasive, or robotic approaches.
- 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: * Adult patients aged 18 years or older * Undergoing isolated CABG * Undergoing CABG with concomitant procedures (e.g., valve repair or replacement) * Undergoing on-pump, off-pump, minimally invasive, or robotic CABG * Procedures performed electively, urgently, or emergently Exclusion Criteria: * Redo CABG when the primary operative record is not available * Patients younger than 18 years
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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 official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a kidney ultrasound scan warn of kidney damage after heart bypass surgery?