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Poor sleep before surgery may slow anesthesia recovery, study hints

NCT ID NCT07675993

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 30, 2026 · Last updated Jul 01, 2026 · Updated 1 time

Summary

This study investigates whether people with sleep disorders before noncardiac surgery take longer to wake up from anesthesia and have a lower quality recovery. Researchers will monitor brain activity during and after surgery in 80 adults, comparing those with poor sleep to those with good sleep. The goal is to understand how sleep health influences anesthesia depth and emergence, which could help personalize anesthesia care.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If sleep problems are shown to slow anesthesia recovery, this could lead to better preoperative sleep screening and tailored anesthesia plans.
What could go wrong
This is a small observational study, so it cannot prove cause and effect. Results may not apply to all surgery types or patient groups.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 80 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2026

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Patients scheduled for elective non-cardiac surgery under general anesthesia at our hospital will be enrolled in this study.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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 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 (SpO₂ \< 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 (SpO₂ \< 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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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

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  3. A doctor treating you

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Contacts and locations

Locations

  • General hospital of Ningxia medical university

    RECRUITING

    Yinchuan, Ningxia, 750001, China