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Recruiting NCT07593794

NCT07593794 QoR-15T in Cardiac Surgery

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Clinical Trial Summary
NCT ID NCT07593794
Status Recruiting
Phase
Sponsor Kocaeli City Hospital
Condition Postoperative Recovery
Study Type OBSERVATIONAL
Enrollment 150 participants
Start Date 2026-05-18
Primary Completion 2026-09-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

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 150 participants in total. It began in 2026-05-18 with a primary completion date of 2026-09-30.

⚠ 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

The objective of this prospective observational cohort study is to evaluate the validity, reliability, and responsiveness of the Turkish version of the Quality of Recovery-15 (QoR-15T) scale in adult patients undergoing elective cardiac surgery. While the QoR-15T has been validated for general surgery in Turkey, its performance remains to be established in high-risk cardiac surgery populations involving cardiopulmonary bypass and intensive care stays.Approximately 150 patients at Kocaeli City Hospital will be enrolled. The study will compare the patients' QoR-15T scores-recorded preoperatively and on the 7th postoperative day-with the Global Recovery Visual Analog Scale (VAS) to determine construct validity.

Eligibility Criteria

Inclusion Criteria: * Adult patients aged 18 years and older. * Patients scheduled for elective cardiac surgery (CABG, valve replacement, or aortic surgery). * Patients capable of understanding and answering the Turkish version of the QoR-15 questionnaire. * Patients who provide written informed consent. Exclusion Criteria: * Emergency surgeries or revision surgeries * Patients with severe cognitive impairment or psychiatric disorders that prevent completion of the scale * Patients who refuse to participate at any stage.

Contact & Investigator

Central Contact

Zeynep Yasemin Tavşanoğlu, MD, DESAIC

✉ zeynepyaseminyilmaz@gmail.com

📞 +902622252700

Frequently Asked Questions

Who can join the NCT07593794 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Postoperative Recovery. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07593794 currently recruiting?

Yes, NCT07593794 is actively recruiting participants. Contact the research team at zeynepyaseminyilmaz@gmail.com for enrollment information.

Where is the NCT07593794 trial being conducted?

This trial is being conducted at Kocaeli, Turkey (Türkiye).

Who is sponsoring the NCT07593794 clinical trial?

NCT07593794 is sponsored by Kocaeli City Hospital. The trial plans to enroll 150 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology