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Study for the Dose-effect Relationship of Propofol and the Quality of Postoperative Recovery in Patients with Insomnia during Perioperative Period

Study for the Dose-effect Relationship of Propofol and the Quality of Postoperative Recovery in Patients with Insomnia during Perioperative Period

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900020935
Enrollment
Unknown
Registered
2019-01-22
Start date
2019-01-21
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

Insomnia

Interventions

Normal Group :propofol
Insomnia Group:Propfol

Sponsors

Department of Anesthesiology, Renji Hospital, Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 65 years old, ASA grade I-II gynecological tracheal intubation of general anesthesia female patients; 2. junior high school and above chemical history; 3. signed the informed consent form;

Exclusion criteria

Exclusion criteria: 1. BMI = 30, patients with obstructive sleep dysfunction; 2. patients suffering from insomnia due to severe cancer pain before surgery; 3. liver and kidney dysfunction; 4. moderate to severe anemia (HGB 180mmHg); 7. anesthesia drug allergy; 8. history of cerebral hemorrhage, brain trauma or surgery.

Design outcomes

Primary

MeasureTime frame
dose-effect relationship of propofol in patients with insomnia;sleep quality postoperatively;—

Secondary

MeasureTime frame
pain postoperatively;anesthesic side reaction;—

Countries

China

Contacts

Public ContactPing Huang

Department of Anesthesiology, Renji Hospital, Shanghai Jiaotong University School of Medicine

apple_h_p@aliyun.com+86 13052237391

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026