NCT07711951

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
400

participants targeted

Target at P75+ for all trials

Timeline
1mo left

Started Jul 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress31%
Jul 2026Aug 2026

First Submitted

Initial submission to the registry

July 14, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

July 17, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

July 20, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2026

Last Updated

July 21, 2026

Status Verified

July 1, 2026

Enrollment Period

1 month

First QC Date

July 14, 2026

Last Update Submit

July 20, 2026

Conditions

Keywords

Cardiac Surgery

Outcome Measures

Primary Outcomes (1)

  • Postoperative Intensive Care Unit Length of Stay

    Postoperative intensive care unit length of stay will be defined as the duration from admission to the intensive care unit following surgery until transfer from the intensive care unit to the hospital ward and will be recorded in days. Patients who die during the intensive care unit stay will not be included in the primary intensive care unit length-of-stay analysis.

    Up to 30 days after surgery

Secondary Outcomes (4)

  • Postoperative Atrial Fibrillation

    Up to 30 days after surgery

  • Acute Kidney Injury

    Up to 30 days after surgery

  • Postoperative Respiratory Failure

    Up to 30 days after surgery

  • 30-Day All-Cause Mortality

    Within 30 days after surgery

Study Arms (1)

Elective Isolated CABG Cohort

Adult patients who underwent elective isolated coronary artery bypass graft surgery between January 1, 2019, and December 31, 2025, and met the predefined eligibility criteria. Cardiopulmonary bypass and aortic cross-clamp durations will be evaluated as continuous exposure variables.

Other: Cardiopulmonary Bypass DurationOther: Aortic Cross-Clamp Duration

Interventions

Aortic cross-clamp duration, defined as the total duration of aortic cross-clamping during elective isolated coronary artery bypass graft surgery and recorded in minutes. This exposure will be evaluated as a continuous variable based on routinely collected operative and perfusion records.

Elective Isolated CABG Cohort

Cardiopulmonary bypass duration, defined as the total duration of cardiopulmonary bypass during elective isolated coronary artery bypass graft surgery and recorded in minutes. This exposure will be evaluated as a continuous variable based on routinely collected perfusion records.

Elective Isolated CABG Cohort

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult patients who underwent elective isolated coronary artery bypass graft surgery at a single tertiary care center between January 1, 2019, and December 31, 2025. All patients meeting the predefined eligibility criteria and with complete electronic medical records required for the study analyses will be included in the retrospective cohort.

You may qualify if:

  • 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

You may not qualify if:

  • Emergency coronary artery bypass graft surgery
  • Concomitant valve surgery
  • Concomitant aortic surgery
  • Reoperation cases
  • Incomplete study-related data
  • Intraoperative death

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fatma Acil

Diyarbakır, Outside of the US, 21070, Turkey (Türkiye)

RECRUITING

Related Publications (1)

  • Anastasiadis K, Antonitsis P, Voucharas C, Apostolidou-Kiouti F, Deliopoulos A, Haidich AB, Argiriadou H. Minimal invasive extracorporeal circulation versus conventional cardiopulmonary bypass in cardiac surgery: a contemporary systematic review and meta-analysis. Eur J Cardiothorac Surg. 2025 Mar 28;67(4):ezaf112. doi: 10.1093/ejcts/ezaf112.

    PMID: 40131383BACKGROUND

MeSH Terms

Conditions

Coronary Artery Disease

Condition Hierarchy (Ancestors)

Coronary DiseaseMyocardial IschemiaHeart DiseasesCardiovascular DiseasesArteriosclerosisArterial Occlusive DiseasesVascular Diseases

Study Officials

  • Fatma Acil, M.D.

    Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Fatma Acil, M.D.

CONTACT

Andaç Dedeoğlu, M.D.

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

July 14, 2026

First Posted

July 17, 2026

Study Start

July 20, 2026

Primary Completion (Estimated)

August 30, 2026

Study Completion (Estimated)

August 30, 2026

Last Updated

July 21, 2026

Record last verified: 2026-07

Locations