Hidden nerve damage may disrupt Heart's electrical activity during surgery
NCT ID NCT07684768
First seen Jul 06, 2026 · Last updated Jul 07, 2026 · Updated 1 time
Summary
This study looks at whether cardiac autonomic neuropathy (nerve damage that affects heart rate control) changes the heart's electrical recovery time (QT interval) in people having coronary artery bypass surgery. Researchers will test nerve function before surgery and measure heart rhythm at several points during and after the operation. The goal is to see if patients with this nerve condition are more likely to have dangerous heart rhythm changes during surgery.
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 cardiac autonomic neuropathy is shown to prolong QT intervals during surgery, it could help doctors identify high-risk patients and adjust monitoring or care to prevent dangerous heart rhythms.
- What could go wrong
- This is a small observational study, not a treatment trial. It can only suggest a link, not prove cause and effect. Results may not apply to all heart surgery patients.
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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60 people
The number who actually took part.
- Started
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Oct 2023
- Finished
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Dec 2024
- 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 scheduled for elective isolated coronary artery bypass grafting (CABG) surgery under general anesthesia at a tertiary care university hospital.
- Ages
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18 to 85 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: * Age ≥18 years. * Scheduled for elective isolated coronary artery bypass grafting (CABG). * Sinus rhythm on preoperative 12-lead electrocardiography. * Ability to undergo preoperative cardiovascular autonomic function assessment using Ewing's cardiovascular reflex tests. * Written informed consent provided. Exclusion Criteria: * Previous cardiac surgery. * Emergency CABG. * Permanent pacemaker implantation. * Atrial fibrillation or other clinically significant cardiac arrhythmias. * Bundle branch block. * Congenital long QT syndrome.
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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.
Contacts and locations
Locations
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Health Science University, Haseki Training and Research Hospital
Istanbul, Turkey (Türkiye)
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Sultangazi Haseki Training and Research Hospital
Istanbul, 34265, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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