Actively Recruiting

Age: 18Years +
All Genders
NCT06888427

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

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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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

CHU de Nice

Nice, Alpes-Maritimes, France, 06003

Actively Recruiting

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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

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