Comparison of Target-Controlled and Manual Total Intravenous Anesthesia in Supratentorial Surgery
Recruiting
N/A
Interventional Study
Postoperative Delirium (POD)
Postoperative Pain
PONV
Burst Suppression
Recovery Period, Anesthesia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 60
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 70 (estimated)
- Sponsor
- Istanbul University - Cerrahpasa · Other
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About This Trial
This study aims to investigate the effect of target-controlled infusion using the Eleveld pharmacokinetic model compared with manually controlled total intravenous anesthesia on the incidence of postoperative delirium in patients undergoing supratentorial surgery. Propofol and remifentanil are administered using either target-controlled or manual infusion techniques according to the study protocol…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adult patients aged 18 to 60 years
* Scheduled for elective supratentorial surgery under general anesthesia
* American Society of Anesthesiologists (ASA) physical status I or II
* Planned total intravenous anesthesia with propofol and remifentanil
* Ability to provide written …
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