Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
80

Summary

Conditions
  • General Anesthesia
  • Intraoperative Dexmedetomidine
  • Postoperative Pain
  • Postoperative Sleep Quality
Type
Observational
Design
Observational Model: OtherTime Perspective: Prospective

Participation Requirements

Age
Between 30 years and 55 years
Gender
Both males and females

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...

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 ?rst 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.

Tracking Information

NCT #
NCT03990987
Collaborators
Not Provided
Investigators
Study Director: Junchao Zhu Shengjing Hospital