Actively Recruiting
Sleep Longitudinal Exploration of the Experience of Patients
Led by Centre Hospitalier Universitaire de Nice · Updated on 2025-04-25
1000
Participants Needed
1
Research Sites
36 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Many epidemiological studies report that insomnia is common after fifty years in the general population but also in the post-operative period of surgery. Preoperatively, sleep quality can be disturbed by fear of general anesthesia and surgery. Postoperatively, it seems to be altered by pain, the ambient environment and night care. Literature shows that the occurrence of post-operative sleep disorders seems to lead to (increased) hypnotic consumption in patients who did not consume them in the pre-operative phase with known risks of dependence. Nowadays , general anesthesia is widely practiced worldwide. However, despite continuous improvement in techniques, a large number of patients still experience poor quality postoperative sleep, even with short-term anesthesia. It therefore appears that general anesthesia disrupts the circadian rhythm of patients, even if the mechanisms are still poorly understood. Thus, sleep deprivation could be responsible of physiological alterations that are still unknown, such as delayed healing or impaired respiratory muscle performance, promoting postoperative complications. The aim of this study is to identify the factors impacting the quality of sleep of patients undergoing scheduled surgery during the first postoperative night. And its implication on the occurrence of drowsiness described by the patient the day after their surgical intervention.
CONDITIONS
Official Title
Sleep Longitudinal Exploration of the Experience of Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female subject aged 18 years or older
- Subject scheduled to undergo surgery under general anesthesia (orthopedic, thoracic, vascular or visceral surgery)
- Subject able to complete a self-administered questionnaire
- Subject having given oral consent
You will not qualify if you...
- Subject wishing to discontinue participation in the study before the end
- Subject for whom the surgical procedure could not be performed after admission to the operating room (whatever the reason)
- Subject for whom the surgical procedure was performed urgently before the date initially scheduled (whatever the reason)
- Subject for whom a serious perioperative complication occurred during the surgical procedure
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU de Nice
Nice, Alpes-Maritimes, France, 06003
Actively Recruiting
Research Team
A
Axel Maurice - Szamburski, MD-PhD
CONTACT
J
Juliana Folgado
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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