| NCT ID | NCT07576920 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Inonu University |
| Condition | Anxiety Postoperative |
| Study Type | OBSERVATIONAL |
| Enrollment | 100 participants |
| Start Date | 2026-05-04 |
| Primary Completion | 2026-08-15 |
Eligibility & Interventions
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 100 participants in total. It began in 2026-05-04 with a primary completion date of 2026-08-15.
⚠ 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
Anxiety is a state of worry and apprehension caused by internal and external threats. High preoperative anxiety levels have been associated with increased anesthetic requirements, higher morbidity, and mortality rates. In adult patients undergoing various surgical procedures, preoperative anxiety rates have been reported to range from 11% to 80%. Most studies show that postoperative anxiety levels are related to preoperative anxiety levels. In patients undergoing general anesthesia, anxiety levels increase a few days after surgery as issues related to recovery and pain become apparent. Patients with high postoperative anxiety levels have also been reported to have a higher rate of medical complications.
Eligibility Criteria
Inclusion Criteria: * ASA 1-2 group patients aged 18-65 years who are liver transplant donors Exclusion Criteria: * Patients with communication problems, those who are illiterate, * Patients do not have sufficient time for the tests, * Patients using sedatives, antidepressants, or antiepileptic drugs, * Patients with cerebrovascular or psychiatric diseases, * Patients with alcohol or substance addiction, * Patients who do not want or cannot undergo the second test
Contact & Investigator
Zekine Begeç, professor
PRINCIPAL INVESTIGATOR
Inonu University Department of Anesthesia
Frequently Asked Questions
Who can join the NCT07576920 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Anxiety Postoperative. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07576920 currently recruiting?
Yes, NCT07576920 is actively recruiting participants. Contact the research team at zekine.begec@inonu.edu.tr for enrollment information.
Where is the NCT07576920 trial being conducted?
This trial is being conducted at Malatya, Turkey (Türkiye).
Who is sponsoring the NCT07576920 clinical trial?
NCT07576920 is sponsored by Inonu University. The principal investigator is Zekine Begeç, professor at Inonu University Department of Anesthesia. The trial plans to enroll 100 participants.
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