Actively Recruiting
Impact of Target Controlled Infusion Estimated Concentration of Propofol on Implicit Memory Formation During Propofol-Remifentanil General Anaesthesia
Led by University of Padova · Updated on 2026-06-08
80
Participants Needed
1
Research Sites
2 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating whether different concentrations of Propofol during Total Intravenous Anaesthesia with Target Controlled Infusion (TIVA-TCI) affect implicit memory formation. This study focuses on how Propofol levels at key points—loss of responsiveness, maintenance, and return of responsiveness—might influence memory during general anaesthesia. The question of memory formation during anesthesia remains debated, with no clear anesthetic or analgesic regimen identified to prevent it. Participants will undergo general anesthesia with TIVA-TCI where 20 common Italian words are played continuously from loss of responsiveness until the end of surgery for one group. Another group will have the same procedure but without hearing the words, to measure the role of chance in memory tests. Propofol concentrations and hypnosis levels, monitored by a Sedline device, will be recorded at specific anesthesia stages. Within 12 to 24 hours after surgery, patients will complete tests including Word Stem Recognition, Free Recall, and Forced Choice Recognition to assess implicit memory formation. The study compares results between those exposed to the words during anesthesia and those who were not. Researchers will analyze these outcomes alongside recorded Propofol concentrations to understand their relationship with memory. Participation involves assessments shortly after surgery, with the overall study lasting from anesthesia through postoperative testing.
CONDITIONS
Brief Title
Impact of Estimated Concentration of Propofol on Implicit Memory Formation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- General anaesthesia with TIVA-TCI
- Female gender
- Age between 18 and 90 years
You will not qualify if you...
- ASA classification greater than III
- Premedication with benzodiazepines
- Neurological or psychiatric disease
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Duration of surgery and anaesthesia
Participants undergo general anaesthesia with Target Controlled Infusion of Propofol while word stimuli are presented to assess implicit memory formation.
1 in-person visit during surgery
Duration - 12 to 24 hours after surgery
Within 12 to 24 hours after surgery, participants complete memory tests to assess implicit memory formation.
1 in-person visit for memory testing
Trial Site Locations
Total: 1 location
1
Treviso Regional Hospital
Treviso, TV, Italy, 31100
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here