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Early Postoperative Pain After Cardiac Surgery

StatusCompleted
PhaseNot specified
Started
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Record History

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  1. Trial completed
    • Site details revised
  2. Sponsor changed: Meltem Ceylan Delice to Antalya Training and Research Hospital
  3. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This observational study will evaluate factors that may be associated with pain during the first 24 hours after open heart surgery. The study will include adult patients who underwent coronary artery bypass grafting (CABG), heart valve surgery, or combined cardiac surgery. Researchers will retrospectively review existing medical records to examine whether patient characteristics, preoperative anxiety and depression, and factors related to surgery and anesthesia are associated with postoperative pain. The study will also evaluate postoperative nausea and vomiting and the need for additional pain medication. No treatment or intervention will be assigned to participants as part of this study. Study data will be collected retrospectively from existing medical records.
Trial Details
NCT Number NCT07804732
Lead Sponsor Antalya Training and Research Hospital
Conditions
(from sponsor)		 Postoperative Nausea and Vomiting (PONV)
Related terms Postoperative Nausea and Vomiting, Postoperative Pain
Enrollment 99 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov