Skip to main content
OpenTrials
Completed

NCT Number: NCT04103528

Effects of Procedure Started in the Morning and Afternoon on Early Postoperative Sleep Function and Postoperative Recovery in Patients Under General Anesthesia

The present study was conducted in laparoscopic hysteromyoma patients, aiming to compare the effects of morning surgery with afternoon surgery on early postoperative sleep function and postoperative recovery under general anesthesia.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–60 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

General hospital of Ningxia medical university

Yinchuan, Ningxia, 750004, China

About this study

The circadian rhythm is an intrinsic timing mechanism generated by endogenous systems to adapt to the external environment, which is closely related to the human sleep-wake cycle. Patients after major surgery are prone to changes in sleep structure and sleep quality, called postoperative sleep disturbances (POSD), which are characterized by the total sleep time reduced, rapid eye movement sleep absent, slow wave sleep shortened, and shallow sleep phase increased, times of wakefulness increased, and highly fragmented sleep. Some studies have shown that POSD can aggravate postoperative pain and fatigue, increase postoperative delirium, cardiovascular adverse events, and even cause accidental death of patients. The investigators don't know whether the early postoperative sleep function and postoperative recovery quality of patients undergoing general anesthesia are affected by surgery in the morning or in the afternoon. The present study was conducted in laparoscopic hysteromyoma patients, aiming to compare the effects of morning surgery with afternoon surgery on early postoperative sleep function and postoperative recovery under general anesthesia.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • aged 18-60 years old.
  • ASA status I or II.
  • BMI 18.5-28 kg/m^2.
  • performed with laparoscopic myomectomy.

Exclusion criteria

  • combining with ovarian disease or ovarian surgery.
  • preoperative Athens Insomnia Scale (AIS) score ≥ 4 points
  • chronic use of sedative, hypnotic, psychotropic drugs.
  • recent night shift, cross-time zone, irregular life routine.
  • suffering from mental illness or hearing, visual impairment, and existing sleep apnea syndrome.
  • patients withdraw, or were unable to complete the trial after surgery.
  • lossed bleeding volume more than 500 ml during surgery.
  • performed procedure time exceeded 2 h.

Treatment and study plan

morning surgery

Other

31 patients will be operated on between 8:00 and 12:00 in the morning.

afternoon surgery

Other

31 patients will be operated on between 14:00 and 18:00 in the afternoon.

Primary outcomes

  1. The incidence of postoperative sleep disturbances by Athens Insomnia Scale

    Time frame: 1 day after the operation

    • Postoperative sleep disturbances were defined as the total score of Athens Insomnia Scale more than 6.
    • The incidence of postoperative sleep disturbances was defined as the percentage of the population with a score greater than 6
  2. The sleep time by bispectral index(BIS) monitor from 21:00 to 06:00 on the first night after surgery

    Time frame: 1 day after the operation

    The sleep time: was defined as the total time of BIS values less than 80 during monitoring.

  3. The sleep efficiency by bispectral index(BIS) monitor from 21:00 to 06:00 on the first night after surgery

    Time frame: 1 day after the operation

    The sleep efficiency: was defined as the ratio of a sleeping time over monitoring time.

  4. The sleep quality by bispectral index(BIS) monitor from 21:00 to 06:00 on the first night after surgery

    Time frame: 1 day after the operation

    The sleep quality: was assessed by the area under curve of BIS (BIS-AUC). The BIS-AUC was calculate using the trapezoidal rule, which used trapezium to approximate the region under a curve and calculate its area (GraphPad Prism Version 5.01; San Diego, California). The smaller BIS-AUC was the better sleep quality.

Secondary outcomes

  1. Postoperative recovery Post-operative Quality Recovery Scale(PQRS)

    Time frame: 1 day before surgery (T0), 30 minutes after end of anesthesia (T1), and 1 day after surgery (T2)

    Postoperative Quality Recovery Scale includes five parts: physiological functions (blood pressure, heart rate, temperature, ventilation rate, maintenance of oxygen saturation, airway maintenance, agitation, consciousness, response), Nociceptive (pain, nausea), emotional (depression, anxious), activities of daily living (ability to stand, walk, eat, dress), cognitive function (orientation, digits forward, digits backward, word list, word generation). According to the recovery situation: the physiological function is divided into three levels (3 points: acceptable, 2: abnormality, 1: extreme abnormality), nociceptive, emotional change according to the degree of Likert 5 scored (5: very satisfactory, 4: satisfactory, 3: general, 2: not satisfied, 1: very dissatisfied), and the activities of daily living are equally divided into three levels (3: easy, 2: difficulty, 1: it can't be done completely), when cognitive function score reaches the preoperative baseline level,it means recovery.

  2. The biochemical indicators

    Time frame: 6am one day before and one day after the surgery

    The levels of melatonin (MT), cortisol, and glulcose in the blood were measured separately by ELISA at 6:00am 1 day before and 1 day after surgery.

Sponsors and collaborators

Lead sponsor

General Hospital of Ningxia Medical University

Other

Registry information

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Sep 25, 2019
Registry last updated
Sep 25, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.