Effects of Preoperative Sleep Disorders on Perioperative Anesthesia Depth and Recovery Quality in Patients Undergoing Noncardiac Surgery
Recruiting
Observational Study
Emergence Time
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Study type
- Observational
- Participants needed
- 80 (estimated)
- Sponsor
- General Hospital of Ningxia Medical University · Other
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About This Trial
A Single-Center, Prospective Observational Cohort Study Comparing Perioperative Electroencephalographic Anesthesia Depth Parameters (Electroencephalographic Index, SE/RE Entropy, Burst Suppression Ratio) Between Patients With Preoperative Sleep Disorders and Those Without; To Identify the Independent Effects of Preoperative Sleep Disorders on the Speed of Electroencephalographic Recovery During Em…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. \- Aged 18 to 65 years, with American Society of Anesthesiologists (ASA) physical status classification Ⅰ-Ⅲ;
2. Elective non-cardiac surgery with an expected operative duration longer than 2 hours;
3. Preoperative Mini-Mental State Examination (MMSE) score ≥ 24;
4. Completion…
Contacts
Li Xin Ni, Doctoral
86-951-674-3252
CONTACT