SBU Antalya Training and Research Hospital
Antalya, 07100, Turkey (Türkiye)
Location status: Recruiting
NCT Number: NCT07804732
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.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Antalya, 07100, Turkey (Türkiye)
Location status: Recruiting
Postoperative pain after cardiac surgery is influenced by multiple patient-related, psychological, surgical, and perioperative factors. The relative contribution of these factors to early postoperative pain and related outcomes remains uncertain.
This retrospective observational cohort study will evaluate factors associated with early postoperative pain in adult patients who underwent open cardiac surgery, including coronary artery bypass grafting, valve surgery, or combined cardiac procedures. Existing medical records will be retrospectively reviewed.
The analysis will examine demographic characteristics, preoperative anxiety and depression, surgical characteristics, and perioperative factors in relation to early postoperative pain. Preoperative anxiety and depression will be evaluated using available Hospital Anxiety and Depression Scale (HADS) scores. Postoperative pain will be assessed using Numeric Rating Scale (NRS) measurements recorded during the first 24 hours after surgery. Postoperative nausea and vomiting and the requirement for additional rescue analgesia will also be evaluated as related postoperative outcomes.
Associations between these clinical and psychological factors and postoperative outcomes will be examined using appropriate statistical analyses. No study-specific treatment or intervention will be assigned to participants, as all study data will be obtained retrospectively from existing medical records.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: First 24 hours after surgery
Postoperative pain will be assessed at rest using the 0-10 Numeric Rating Scale (NRS), where 0 indicates no pain and 10 indicates the worst pain. NRS scores recorded at 0, 3, 6, 12, and 24 hours after the initial postoperative assessment in the intensive care unit will be used to calculate the mean pain score (NRSmean) for the first 24 postoperative hours.
Contact information is provided by the study sponsor or research team.
Meltem Ceylan Delice
Other Gov
Early Postoperative Pain and Related Outcomes After Cardiac Surgery: A Retrospective Cohort Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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