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โ† Trials
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Effects of Preoperative Sleep Disorders on Perioperative Anesthesia Depth and Recovery Quality in Patients Undergoing Noncardiac Surgery

Recruitingn/aAges 18 Years - 65 YearsAllGeneral Hospital of Ningxia Medical University
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In plain words

What the trial is, and whether it could suit you

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 Emergence, Electroencephalographic Status at Extubation, Intra-PACU Electroencephalographic Fluctuations, and Quality of Emergence.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: 1. \- Aged 18 to 65 years, with American Society of Anesthesiologists (ASA) physical status classification โ… -โ…ข; 2. Elective non-cardiac surgery with an expected operative duration longer than 2 hours; 3. Preoperative Mini-Mental State Examination (MMSE) score โ‰ฅ 24; 4. Completion of the Pittsburgh Sleep Quality Index (PSQI) assessment 1 day before surgery; 5. Absence of severe cardiac, hepatic, renal or cerebral diseases, and no history of psychiatric or neurological disorders; 6. Voluntary provision of written informed consent. Exclusion Criteria: 1. Preoperative severe cognitive dysfunction, history of traumatic brain injury or stroke; 2. Long-term regular use of sedative-hypnotics, antidepressants or antipsychotics; 3. Intraoperative massive hemorrhage, cardiac arrest, or severe hypoxemia (SpOโ‚‚ \< 90% lasting for more than 5 minutes); 4. Inability to cooperate with EEG monitoring or scale evaluation; 5. Pregnancy or breastfeeding status. Drop-out Criteria : 1. Cancellation of scheduled surgery/anesthesia or postoperative admission to the intensive care unit (ICU); 2. Patient withdrawal of study participation; 3. Intraoperative massive hemorrhage, cardiac arrest, or severe hypoxemia (SpOโ‚‚ \< 90% lasting for more than 5 minutes); 4. Development of severe postoperative complications; 5. Incomplete data collection or voluntary trial withdrawal.
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What it tests

  • Exposed cohort (sleep disorder group)
  • Control cohort (non-sleep disorder group)
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Where

1 site
General hospital of Ningxia medical university
Yinchuan, China
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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