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Impact of Intraoperative Hemodynamic Instability on Outcomes in Cardiac Surgery

StatusCompleted
PhaseNot specified
Started
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Record History

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  1. Minor Trial completed Show 6 more changesShow less
    • Final enrollment: 351 participants (planned 230)
    • Study completion date changed from estimate of Sep 5, 2026 to Sep 20, 2026
    • Eligibility criteria expanded, about 11 words
    • Site details revised
    • Publications: details revised at 3 of 3 entries
    • Study description expanded, about 2 words
  2. Minor Re-verified, no change to tracked fieldsv4
  3. Notable Primary completion pushed from Jan 20, 2026 to Aug 20, 2026
    • Study completion pushed from Feb 5, 2026 to Sep 5, 2026
    v3
  4. Minor Re-verified, no change to tracked fieldsv2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Intraoperative hemodynamic instability (IOHI) is a common occurrence during cardiac surgery and is associated with organ hypoperfusion. However, the specific impact of IOHI on composite adverse outcomes remains unclear. This prospective cohort study aims to evaluate the association between intraoperative hemodynamic instability (defined as MAP \< 65 mmHg or vasopressor requirement) and major postoperative complications (Delirium, Acute Kidney Injury, Stroke, or Mortality) in adult patients undergoing elective cardiac surgery with cardiopulmonary bypass.
Trial Details
NCT Number NCT07324694
Lead Sponsor Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
Conditions
(from sponsor)
Cardiac Surgery, Intraoperative Hemodynamic Instability, Postoperative Complication, Acute Kidney Injury, Postoperative Delirium (POD)
Related terms Acute Kidney Injury, Emergence Delirium, Postoperative Complications
Enrollment 351 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov