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Effect of a single subanesthetic dose of Esketamine on postoperative mood and pain in patients undergoing unilateral modified radical mastectomy under intravenous aspiration combined with general anesthesia: a randomized, controlled, double-blind trial

Effect of single subanesthetic dose of Esketamine on postoperative mood and pain in patients undergoing modified radical operation for unilateral breast cancer under intravenous aspiration combined with general anesthesia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057028
Enrollment
Unknown
Registered
2022-02-26
Start date
2022-03-01
Completion date
Unknown
Last updated
2023-09-26

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

Conditions

Mammary cancer

Interventions

Group E:Intravenous injection of 0.25mg/kg esmketamine
Group N:Intravenous injection of equal volume normal saline

Sponsors

Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Premenopausal adult women; 2. Able to fill out the depression rating form under guidance; 3. ASA ?- ?; 4. Preoperative radiotherapy and chemotherapy were not performed; 5. Those who meet the ethical requirements, voluntarily undergo the test and sign the informed consent; 6. Have not participated in other clinical drug trials within the last month.

Exclusion criteria

Exclusion criteria: 1. Anti-depression treatment within the last 2 months; 2. Previous personality disorder, intellectual impairment, brain injury or brain disease, combined with schizophrenia, mania and other mental diseases; 3. Combination of immune system diseases, or the use of drugs that have a significant effect on the immune system; 4. Pregnancy or lactation; 5. Alcohol addiction; 6. Hypertension patients with poor blood pressure control after treatment or without regular treatment; 7. Glaucoma patients; 8. Patients with intracranial tumor; 9. Patients with cerebrovascular diseases; 10. Allergic to research drug ingredients; 11. Chronic use of sedatives and painkillers.

Design outcomes

Primary

MeasureTime frame
Patient Health Questionnaire-9 (PHQ-9) Score;Visual Analogue Scale Score;

Secondary

MeasureTime frame
Concentration of BDNF in serum;

Countries

China

Contacts

Public ContactHuang Wan

Sun Yat-sen University Cancer Center

huangwan@sysucc.org.cn+86 20 87343060

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026