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Effects of different doses of esketamine preemptive analgesia on immune function, inflammatory response and prognosis in breast cancer patients

Effects of different doses of esketamine preemptive analgesia on immune function, inflammatory response and prognosis in breast cancer patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057226
Enrollment
Unknown
Registered
2022-03-04
Start date
2022-03-20
Completion date
Unknown
Last updated
2023-10-09

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

Conditions

breast cancer

Interventions

L-Esk group: low-dose esketamine group:Esketamine 0.25 mg/kg was administered 5 min before induction of anesthesia
M-Esk group: medium-dose esketamine group :Esketamine 0.5 mg/kg was administered 5 min before induction of anesthesi
H-Esk group: high-dose esketamine group:Esketamine 1 mg/kg was administered 5 min before induction of anesthesia
Group C: control group:Administer an equal dose of normal saline 5 min before induction of anesthesia

Sponsors

Cancer Hospital of General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Female aged 30 to 65 years; 2. ASA classification I or II; 3. Body Mass Index (BMI) of 18-29 kg/m2; 4. Breast cancer patients who were diagnosed with breast cancer by mammography, puncture examination and breast color ultrasound and underwent unilateral radical mastectomy.

Exclusion criteria

Exclusion criteria: 1. Those who have had a history of breast surgery; 2. Patients diagnosed with inflammatory breast cancer; 3. Those with severe heart, lung, liver and kidney dysfunction; 4. Those with a history of opioid addiction; 5. Patients with metastatic breast tumors; 6. Those who received neoadjuvant chemotherapy before surgery; 7. Those with chronic pain disease; 8. Patients with mental illness; 9. Suffering from immune system diseases, or using drugs that have obvious effects on the immune system.

Design outcomes

Primary

MeasureTime frame
T lymphocyte subtypes (CD3+, CD4+ and CD8+);CD4+/CD8+ ratio and percentage of NK cells;Blood routine (peripheral blood neutrophil, lymphocyte, monocyte, platelet );Inflammatory cytokines: IL-6, IL-10, IL-1ß, TNF-a;

Secondary

MeasureTime frame
Record recurrence, metastasis and treatment;Anxiety, Depression;15-item quality of recovery rating scale, QoR-15;

Countries

China

Contacts

Public ContactXuexin Chen

Cancer Hospital of General Hospital of Ningxia Medical University

chenxuexin2637@163.com+86 13995001031

Outcome results

None listed

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