A study on postoperative sleep and rehabilitation in patients undergoing sinus surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400090991

Enrollment

Unknown

Registered

2024-10-17

Start date

2023-08-07

Completion date

Unknown

Last updated

2024-10-21

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

Conditions

postoperative sleep disorders

Interventions

control group:none

Esketamine group:Extra intravenous injection of 0.5mg/kg ketamine during induction period

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age 18-65 years old, ASA grade I-III; Patients undergoing sinus surgery under elective general anesthesia.

Exclusion criteria

Exclusion criteria: (1) Body mass index BMI>30 (2) Preoperative Pittsburgh Sleep Quality Index PSQI>7 points (3) Contraindications or severe allergies to ketamine (4) Long term use of benzodiazepines or antipsychotic drugs (5) Cognitive impairment or inability to communicate (6) The patient refused to participate in this study

Design outcomes

Primary

Measure	Time frame
Asens Sleep Scale;	—

Secondary

Measure	Time frame
Self Rating Anxiety Scale;SNOT-20;VAS;Adverse reactions;	—

Countries

China

Contacts

Public ContactChen Jing

The First Affiliated Hospital of Guangxi Medical University

352880721@qq.com+86 136 0781 5280

Outcome results

None listed

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