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Effect of preoperative sleep quality on target concentration of propofol and postoperative sleep function in patients undergoing painless gastroscopy

Effect of preoperative sleep quality on target concentration of propofol and postoperative sleep function in patients undergoing painless gastroscopy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100045332
Enrollment
Unknown
Registered
2021-04-12
Start date
2021-04-19
Completion date
Unknown
Last updated
2021-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relationship between sleep quality and anesthesia

Interventions

Sleep Disorders Group:Target controlled infusion of propofol
Normal sleep group:Target controlled infusion of propofol

Sponsors

General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 64 Years

Inclusion criteria

Inclusion criteria: Outpatient patients undergoing painless gastroscopy, age 45-64 years old, body mass index 18.5-30 Kg/m^2, ASA I or II.

Exclusion criteria

Exclusion criteria: Mental disease, postoperative digestive tract tumor, poor control of hypertension, cardiopulmonary insufficiency, morbid obesity, sleep apnea syndrome, digestive tract obstruction, severe liver and kidney insufficiency, acute upper respiratory infection, and people who need to care for children/the elderly at night or work night shifts.

Design outcomes

Primary

MeasureTime frame
Plasma target concentration of propofol;Sleep function after painless gastroscopy;

Secondary

MeasureTime frame
Anesthesia-related adverse reactions;Complications of anesthesia;Satisfaction of endoscopists;Satisfaction of patient;

Countries

China

Contacts

Public ContactQiu Yuxue

General Hospital of Ningxia Medical University

xueer3864@163.com+86 13639571051

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026