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Effects of sub-anaesthetic dose of esketamine on stress response and immune function in patients with breast cancer during perioperative period

Effects of sub-anaesthetic dose of esketamine on stress response and immune function in patients with breast cancer during perioperative period

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044883
Enrollment
Unknown
Registered
2021-03-31
Start date
2021-06-01
Completion date
Unknown
Last updated
2021-11-02

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

Conditions

Stress response and immune function

Interventions

Observation group:Patients in the observation group were given intravenous injection of 0.5mg/kg esketamine before induction of anesthesia, and diluted with 0.25mg/kg/h esketamine to 50ml intravenous
Control group:The PCIA regimen of the control group was Kaifen 100mg+ondansetron 16mg+esketamine 100mg.

Sponsors

Women and Children's Hospital, School of Medicine, Xiamen university
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosed stage I and stage II breast cancer by imaging features and histopathological examination; 2.American Association of Anesthesiologists (ASA) grade I-II; 3.There are no obvious abnormalities in organs such as heart, liver, kidney, etc. Lesions; 4.The expected survival time is> 6 months, and the Karnofsky score is > 60 points.

Exclusion criteria

Exclusion criteria: 1.Recent use of hormonal drugs; 2.Confusion, mental illness; 3.Preoperative chemotherapy and radiotherapy; 4.Recurrence of breast cancer, combined with other malignant tumors; 5.Severe electrolyte imbalance; 6.Long-term use of sedative or analgesic drugs; 7.Pregnancy or lactation stage.

Design outcomes

Primary

MeasureTime frame
Angiotensin-II (ANG-II);Aldosterone (ALD);Cortisol;Tumor Necrosis Factor (TNF)-a;Total T cells in peripheral blood;B lymphocytes;NK cells;The amount of sufentanil, the amount of remifentanil, the residence time in the recovery room, the time of extubation from anesthesia, and the time of awakening from anesthesia were recorded for the two groups of patients during surgery.;Adverse reactions in the wake of the two groups of patients after the operation: chills, restlessness, tachycardia, increased secretions, respiratory depression, hypertension, hallucinations;

Countries

China

Contacts

Public ContactJia Junxiang

Women and Children's Hospital, School of Medicine, Xiamen university

ybmzjjx@126.com+86 15980965934

Outcome results

None listed

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