NCT07711951Completed
CPB and Aortic Cross-Clamp Durations and ICU Length of Stay After CABG Retrospective Observational Cohort Study
Association of Cardiopulmonary Bypass and Aortic Cross-Clamp Durations With Intensive Care Unit Length of Stay in Elective Isolated Coronary Artery Bypass Graft Surgery: A Retrospective Observational Cohort Study
Source: ClinicalTrials.gov · Last updated 2 Sept 2026
Brief summary (registry, in English)
Cardiopulmonary bypass (CPB) and aortic cross-clamp (ACC) durations are important intraoperative factors that may influence postoperative recovery following coronary artery bypass graft (CABG) surgery. Prolonged CPB and ACC durations may be associated with increased postoperative morbidity and extended intensive care unit (ICU) stay. This retrospective observational cohort study aims to evaluate the independent associations of CPB and ACC durations with postoperative ICU length of stay in adult patients undergoing elective isolated CABG surgery. Electronic medical records of eligible patients who underwent surgery between January 1, 2019, and December 31, 2025, at a single tertiary care center will be retrospectively reviewed. Multivariable regression analyses will be performed to assess these associations after adjustment for clinically relevant potential confounders.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 387 (actual)
- First submitted
- 14 Jul 2026
- Start date
- 20 Jul 2026
- Primary completion date
- 21 Aug 2026
- Lead sponsor
- Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
- Diseases
- Coronary artery disease
- NCT number
- NCT07711951
What you commit to
- Study type: Observational
- Participants enrolled: 387
- From 20 Jul 2026 to the primary completion date, 21 Aug 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Emergency coronary artery bypass graft surgery
- Concomitant valve surgery
- Concomitant aortic surgery
Other
- Reoperation cases
- Incomplete study-related data
- Intraoperative death
Who the study is looking for
- Age 18 years or older
- Underwent elective isolated coronary artery bypass graft surgery
- Surgery performed between January 1, 2019, and December 31, 2025
- Availability of complete electronic medical records required for the study analyses
Age in the registry: 18 years to - · Sex: All
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Fatma Acil Coordinator of this site? Confirm its status | Diyarbakır | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.