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Effect of esketamine on postoperative sleep quality in female patients undergoing laparoscopic surgery

Effect of esketamine on postoperative sleep quality in female patients undergoing laparoscopic surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113859
Enrollment
Unknown
Registered
2025-12-04
Start date
2025-12-10
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Dyssomnia

Interventions

Control group ( group C ):Group C was given intravenous injection of normal saline with the same volume of esketamine as group S during anesthesia induction.
Esketamine group ( S group ):In group S, esketamine 0.3 mg / kg was intravenously injected during anesthesia induction.

Sponsors

Huzhou Maternity & Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age 25 ~ 60 years old, ASA grade I ~ II.

Exclusion criteria

Exclusion criteria: Patients with a history of mental illness or chronic pain, long-term use of sedatives or opioids, and allergy to the study drug, BMI >=30 kg / m2.

Design outcomes

Primary

MeasureTime frame
The Pittsburgh Sleep Quality Index ( PSQI ) scores at 1, 3 and 7 days after operation were recorded.;The visual analogue pain score ( VAS ) at 6 h and 24 h after operation was recorded.;

Secondary

MeasureTime frame
Total dosage of sufentanil during operation;

Countries

China

Contacts

Public ContactDu Rui

Huzhou Maternity & Child Health Care Hospital

26100559@qq.com+86 152 6824 3201

Outcome results

None listed

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