The Effect of Intraoperative Use of Dexmedetomidine During the Daytime Operation vs the Nighttime Operation on Postoperative Sleep Quality and Pain Under General Anesthesia

Last updated: September 17, 2019
Sponsor: Shengjing Hospital
Overall Status: Active - Recruiting

Phase

N/A

Condition

Post-surgical Pain

Chronic Pain

Pain

Treatment

N/A

Clinical Study ID

NCT03990987
Dexmedetomidine and sleep
  • Ages 30-55
  • All Genders

Study Summary

General anesthesia is a medically induced state of low reactivity consciousness which is similar to natural sleep. Some studies found that general anesthesia as an independent risk factor could result in a desynchronization of the circadian time structure and cause postoperative sleep disorders characterized by reduced rapid eye movement (REM) and slow wave sleep (SWS), which have significant deleterious impacts on postoperative outcomes, such as postoperative fatigue, severe anxiety and depression, emotional detachment and delirium, and even pain sensitivity or postoperative pain of patients.Clinical trials have already proved that intraoperative use of dexmedetomidine (DEX) for general anesthesia, a highly selective alpha-2 adrenergic agonist, was able to improve sedative and analgesia effects and promote sleep quality (by decreasing stage N1 sleep, increasing stage N2 sleep and sleep efficiency). However, Wenfei Tan et al reported that with the deeper sedative state provided by DEX in the daytime, the elderly male patients undergoing TURP under spinal anesthesia suffered worse sleep on the night of surgery. Thus, what the effect of intraoperative using DEX at different time periods under general anesthesia on postoperative sleep quality and pain will be needs further study.

Eligibility Criteria

Inclusion

Inclusion Criteria: age between 30 and 55 years American Society of Anaesthesiologists physical status I or II.

Exclusion

Exclusion Criteria: cardiovascular disease long term use of analgesia preoperative heart rate (HR) less than 50beats/min second- or third-degree atrioventricular block sleep disorder sleep apneasyndrome history of abnormal operation or anesthesia recovery psychosis or a patient with alanguage communication disorder not willing to cooperate with the experimenter.

Study Design

Total Participants: 75
Study Start date:
June 15, 2019
Estimated Completion Date:
December 31, 2019

Study Description

patients scheduled for elective laparoscopic abdominal surgeries under general anesthesia were enrolled. Patients were randomized to receive operation in the D group (8:00-12:00) and the N group (18:00-22:00). The Portable Sleep Monitor (PSM) was performed on the following 3 nights: the night before surgery (Sleep1), the first night after surgery (Sleep 2), and the third night after surgery (Sleep 3). Postoperative pain scores using visual analogue scoring scale, subjective sleep quality using the Athens Insomnia Scale, total dose of general anesthetics and PCA pump press numbers were also recorded.

Connect with a study center

  • shengjing hospital of China medical university

    Shenyang, Liao Ning 110004
    China

    Active - Recruiting

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