NCT07557433 Relationship Between Induction Burst Suppression and Bispectral Index
| NCT ID | NCT07557433 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Amasya University |
| Condition | Bispectral Index Monitoring |
| Study Type | OBSERVATIONAL |
| Enrollment | 200 participants |
| Start Date | 2026-07-01 |
| Primary Completion | 2027-06-01 |
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 200 participants in total. It began in 2026-07-01 with a primary completion date of 2027-06-01.
⚠ 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 purpose of this study is to understand whether certain brain activity patterns that can appear at the beginning of anesthesia are related to how deep anesthesia remains during the operation. The main question of the study is: Do patients who show a pattern called burst suppression during the start of anesthesia experience deeper anesthesia during surgery? Patients who are scheduled for elective surgery under total intravenous anesthesia (TIVA) may take part in this study. During the operation, brain activity will be monitored using a sensor placed on the forehead (Bispectral Index, BIS monitor), which is already commonly used during anesthesia. Information such as BIS values and the doses of anesthesia medications given during the operation will be recorded. Participation in this study will not change the type of anesthesia or the routine care that patients receive during surgery. The study only involves recording and analyzing information collected during standard anesthesia monitoring.
Eligibility Criteria
Inclusion Criteria: * Age between 18 and 75 years * American Society of Anesthesiologists (ASA) physical status I-III * Scheduled for elective surgery * Surgery planned to be performed under total intravenous anesthesia (TIVA) Exclusion Criteria: * Presence of neurological disease * Chronic use of sedative medications or antiepileptic drugs * Severe hepatic or renal dysfunction * Intraoperative administration of ketamine or dexmedetomidine
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07557433 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Bispectral Index Monitoring. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07557433 currently recruiting?
Yes, NCT07557433 is actively recruiting participants. Contact the research team at bulentmericcam@gmail.com for enrollment information.
Where is the NCT07557433 trial being conducted?
This trial is being conducted at Amasya, Turkey (Türkiye), Izmir, Turkey (Türkiye).
Who is sponsoring the NCT07557433 clinical trial?
NCT07557433 is sponsored by Amasya University. The trial plans to enroll 200 participants.