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The effect of esketamine combined with dexmedetomidine on postoperative sleep after laparoscopic gynecological surgery

The effect of esketamine combined with dexmedetomidine on postoperative sleep after laparoscopic gynecological surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116546
Enrollment
Unknown
Registered
2026-01-12
Start date
2026-01-12
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Laparoscopic gynecological surgery

Interventions

Control group (Group A):After anesthesia induction, intravenous infusion of isotonic normal saline was initiated.
The dexmedetomidine group (Group B):After anesthesia induction, intravenous infusion of dexmedetomidine at 0.4 µg/kg/h and an equal volume of normal saline was administered until ten minutes before th
Esketamine group (Group C):After anesthesia induction, intravenous infusion of esketamine at a rate of 0.3 mg/kg/h was administered along with an equal volume of normal saline until ten minutes before
The dexmedetomidine combined with esketamine group (Group D):After anesthesia induction, intravenous infusion of esketamine at 0.3 mg/kg/h and dexmedetomidine at 0.4 µg/kg/h was administered until ten

Sponsors

Jinjiang Municipal Hospital (Shanghai Sixth People's Hospital Fujian )
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Age between 18 years and 65 years; (2) BMI ranging from 18.5 to 28 Kg/m^2; (3) Preoperative PSQI score less than 7 points; (4) ASA classification as grade I to II; (5) Elective surgery; (6) No allergy to trial-related drugs.

Exclusion criteria

Exclusion criteria: (1) Those with diagnosed mental disorders or intellectual disabilities before the surgery; (2) Patients who cannot complete the self-assessment questionnaire or cannot cooperate with follow-up due to various reasons; (3) Patients who were under drug-induced hypnosis before the surgery; (4) Patients with bradycardia or atrioventricular conduction block before the surgery; (5) Patients with a high risk of severe hypertension or intracranial pressure elevation before the surgery.

Design outcomes

Primary

MeasureTime frame
The Ainsworth Insomnia Scale on the 1st and 3rd days after the operation;

Secondary

MeasureTime frame
On the first day after the surgery, QoR-15;Extubation time;Usage of vasoactive drugs during the operation;The total dose of propofol and remifentanil used during the operation;Postoperative VAS score;Preoperative and postoperative Lac and Glu blood gas values;Heart rate (HR) and mean arterial pressure (MAP) before the operation, 5 minutes, 15 minutes, and 30 minutes after extubation;

Countries

China

Contacts

Public ContactWang Qiufen

Jinjiang Municipal Hospital (Shanghai Sixth People's Hospital Fujian )

27225105@qq.com+86 157 5987 0926

Outcome results

None listed

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