NCT07804732 Early Postoperative Pain After Cardiac Surgery
| NCT ID | NCT07804732 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Antalya Training and Research Hospital |
| Condition | Postoperative Nausea and Vomiting (PONV) |
| Study Type | OBSERVATIONAL |
| Enrollment | 99 participants |
| Start Date | 2026-08-10 |
| Primary Completion | 2026-09-05 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 99 participants in total. It began in 2026-08-10 with a primary completion date of 2026-09-05.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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.
Eligibility Criteria
Inclusion Criteria: * Age ≥18 years * Underwent open cardiac surgery, including coronary artery bypass grafting (CABG), valve surgery, or combined cardiac surgery * Complete perioperative and postoperative pain data available in the medical records Exclusion Criteria: * Incomplete medical records * Reoperation within the first 24 postoperative hours * Chronic opioid use * Cognitive impairment
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07804732 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Postoperative Nausea and Vomiting (PONV). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07804732 currently recruiting?
Yes, NCT07804732 is actively recruiting participants. Contact the research team at ceylanmeltem93@gmail.com for enrollment information.
Where is the NCT07804732 trial being conducted?
This trial is being conducted at Antalya, Turkey (Türkiye).
Who is sponsoring the NCT07804732 clinical trial?
NCT07804732 is sponsored by Antalya Training and Research Hospital. The trial plans to enroll 99 participants.