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Effect of Esketamine Hydrochloride on Postoperative Anxiety and Depression in Patients Undergoing Multiple Wound Repair Operations

Effect of Esketamine Hydrochloride on Postoperative Anxiety and Depression in Patients Undergoing Multiple Wound Repair Operations

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078540
Enrollment
Unknown
Registered
2023-12-12
Start date
2023-12-15
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Anxiety and depression

Interventions

Test group:After induction for 5 minutes, continue to pump 0.2-0.3 mg/kg of Esketamine for 20 minutes
Control group:Continuously pump physiological saline 0.2-0.3mg/kg for 20 minutes after induction for 5 minutes

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Age 18 or above; (2) ASA grading 1-2, without other serious systemic diseases; (3) Patients who have undergone more than 2 trauma repair surgeries; (4) Patients with preoperative scores of = 22 on the Montgomery Depression Rating Scale and = 10 on the PHQ-9 Scale; (5) Voluntarily sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with other mental illnesses; (2) Patients with contraindications to ketamine use or a history of allergy to other opioid drugs; (3) Patients with a history of cerebral infarction; (4) Patients who have used hormones within the past month; (5) Patients who have been drinking excessively or taking sedatives and analgesics for a long time; (6) Patients with diabetes or rheumatic immune diseases; (7) Refusing to participate in the trial patients; (8) Patients with preoperative hemoglobin below 90g/L; (9) A clear diagnosis of depression in patients before surgical trauma; (10) Patients expected to enter the ICU after surgery; (11) Patients with MMSE score<18;

Design outcomes

Primary

MeasureTime frame
Three days after surgery, the Montgomery Eisberg depression score decreased by 50% compared to baseline;

Secondary

MeasureTime frame
After treatment, the Montgomery Eisberg depression score was = 10;PHQ-9 ;Athens insomnia scale;Hospital anxiety and depression scale;

Countries

China

Contacts

Public ContactQiang Fu

Chinese PLA General Hospital

13691436328@163.com+86 136 9143 6328

Outcome results

None listed

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