Actively Recruiting

Age: 18Years - 90Years
FEMALE
ID06497855

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

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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

Age: 18Years - 90Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • General anaesthesia with TIVA-TCI
  • Female gender
  • Age between 18 and 90 years
Not Eligible

You will not qualify if you...

  • ASA classification greater than III
  • Premedication with benzodiazepines
  • Neurological or psychiatric disease

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

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

Long-term Monitoring

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

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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

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