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The effect of esketamine on postoperative immune function and long-term prognosis in patients undergoing radical surgery for esophageal cancer

The effect of esketamine on postoperative immune function and long-term prognosis in patients undergoing radical surgery for esophageal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081487
Enrollment
Unknown
Registered
2024-03-04
Start date
2024-03-07
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

esophageal cancer

Interventions

control group:The control group received an equivalent volume of 0.9% saline for the same duration.
esketamine group:After induction, the esketamine group received a continuous infusion at 0.02 mgkg-1hr-1 until the end of surgery, and PCIA (1 mg/kg esketamine+sufentanil 1.5) µg/kg).

Sponsors

The Fourth Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Age = 18 years old, regardless of gender; (2) Patients planning to undergo elective radical surgery for esophageal cancer; (3) ASA score levels I-III; (4) Voluntarily sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Expected hospitalization time<48 hours; (2) Individuals who are known to be allergic to the active ingredients or excipients of ketamine hydrochloride injection; (3) Severe consciousness disorders or the presence of mental system diseases; (4) Have a serious history of cardiovascular disease (presence of congestive heart failure, severe angina attacks, or unstable angina or myocardial infarction within 6 months); (5) Pregnant or lactating patients; (6) Patients who have received immunosuppressive therapy (such as PD-1 inhibitors), received hormone therapy within 6 months, or have obvious symptoms of infection; (7) Refusal to sign informed consent form

Design outcomes

Primary

MeasureTime frame
CD3+T lymphocyte percentage;

Secondary

MeasureTime frame
T4 lymphocyte percentage;T8 lymphocyte percentage;CD4/CD8 lymphocyte subgroup ratio;B lymphocyte percentage;NK cell percentage;Postoperative pain VAS score and analgesic remedy use;Pulmonary complications;Regional lymph node metastasis, local recurrence, or distant metastasis within 2 years after surgery;CRP ;TNF-a ;IL-6; Sleep quality score ;and postoperative recovery quality within 30 days after surgery;

Countries

China

Contacts

Public ContactChao Li

The Fourth Hospital of Hebei Medical University

jysylichao1976@163.com+86 138 3111 0738

Outcome results

None listed

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