Actively Recruiting
Dreams or Implicite Memorization Under OFA
Led by Centre Hospitalier Universitaire Saint Pierre · Updated on 2025-02-12
40
Participants Needed
1
Research Sites
2 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to observe and evaluate the occurrence of connected awareness during and after general anesthesia without the use of opioids in patients undergoing laparoscopic robotic surgery. It focuses on measuring explicit and implicit memorization during the procedure and assessing patients' postoperative well-being, including pain levels, analgesic use, satisfaction, hospitalization duration, and early mobilization. The study is conducted by Centre Hospitalier Universitaire Saint Pierre and includes adults aged 18 to 75 years with specific health criteria. Participants will receive general anesthesia without opioids, and their experience of connected consciousness after intubation will be monitored. The study does not involve experimental treatments but carefully observes the anesthesia process and patient responses. Data on pain using visual scales, medication consumption, satisfaction through the EVAN scale, and recovery milestones will be collected from the operating room through one week post-surgery. During the study, participants will be assessed for implicit and explicit memorization from the operating room until one week after surgery. Researchers will track postoperative pain, analgesic use, satisfaction levels, hospitalization length, and timing of first mobilization. The study involves regular monitoring to evaluate these outcomes and support understanding of consciousness and recovery under opioid-free anesthesia in this patient group.
CONDITIONS
Brief Title
Dreams or Implicite Memorization Under OFA
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Undergoing laparoscopic robotic surgery
- ASA score between 1 and 3
- Age between 18 and 75 years
You will not qualify if you...
- Having neurological or psychiatric diseases
- Having memory disorders
- History of head trauma
- Hearing disorders
- Current or past use of medications affecting the central nervous system
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 - From the operating room to 1 week after surgery
Participants undergo assessments related to their laparoscopic robotic surgery and initial monitoring for memorization incidents.
1 surgery visit and multiple monitoring assessments up to 1 week post-surgery
Trial Site Locations
Total: 1 location
1
CHU Saint Pierre
Brussels, Belgium, 1000
Actively Recruiting
Research Team
F
Florent Postal, Md
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Frequently Asked Questions
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