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Effect of esmketamine on postoperative sleep quality of patients undergoing laparoscopic gynecological surgery

Effect of esketamine on postoperative sleep quality of patients undergoing laparoscopic gynecological surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048587
Enrollment
Unknown
Registered
2021-07-11
Start date
2021-10-01
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

Gynecological laparoscopic surgery

Interventions

experimental group:esketamine
Control group:No

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Select patients for elective gynecological laparoscopic surgery; 2. Aged 18 to 60 years; 3. BMI 18-25.0 kg/m2; 4. ASA I or II grade.

Exclusion criteria

Exclusion criteria: Hypertension and diabetes, preoperative language and cognitive impairment, sleep problems, past serious mental or neurologic history, drug abuse or psychotic drug abuse, long-term use of steroid drugs, hormone drugs, recent major operation history, severe vision and hearing impairment.

Design outcomes

Primary

MeasureTime frame
Postoperative sleep quality;Static and dynamic VAS scores;?????????? Intraoperative opioid consumption;

Secondary

MeasureTime frame
adverse reaction;postoperative anxiety and depression scores;expore the risk fators of sleep disturbance;

Countries

China

Contacts

Public ContactYang Jianjun

The First Affiliated Hospital of Zhengzhou University

qd15136760769@163.com+86 13783537619

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026