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Analgesic and myocardial protection effects of different doses of esketamine as adjuvant for anterior serratus muscle plane block in patients with coronary heart disease and lung cancer

Analgesic and myocardial protection effects of different doses of esketamine as adjuvant for anterior serratus muscle plane block in patients with coronary heart disease and lung cancer

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400082322
Enrollment
Unknown
Registered
2024-03-26
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Lung Cancer

Interventions

A:0.33% ropivacaine block on the anterior serratus muscle plane
B:0.33% ropivacaine block on the anterior serratus muscle plane + 20 mg esketamine
C:0.33% ropivacaine block on the anterior serratus muscle plane + 30 mg esketamine

Sponsors

the First Affiliated Hospital of Hebei North University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients who plan to undergo thoracoscopic lung cancer with concomitant coronary heart disease; (2) ASA grade II-III, age>45 years but<75 years old; BMI (18-25) kg/m2; Surgical time is 2-4 hours; (3) NYHA classification level I to II; (4) Patients undergoing elective surgery must have their endotracheal tube removed after surgery.

Exclusion criteria

Exclusion criteria: (1) Individuals who are known to be allergic to ketamine and other medications used in this study; (2) Individuals who have experienced angina and severe heart failure in the past three months; (3) Patients with severe liver, kidney or metabolic diseases before surgery; (4) Patients with sinus bradycardia and cardiac conduction system block; (5) Severe electrolyte imbalance and acid-base imbalance; (6) Long term use of sedative or psychiatric drugs; (7) Intraoperative bleeding volume>800ml, excluding cases exceeding 20% of circulating blood volume; (8) Not willing to accept the operator of this experiment.

Design outcomes

Primary

MeasureTime frame
First wake-up time;High-sensitivity cardiac troponin T ;Cardiac troponin T ;High-sensitivity C-reactive protein;Interleukin-6;Interleukin-10;Vas score;

Secondary

MeasureTime frame
Adverse event ;

Countries

China

Contacts

Public ContactChen Yanlin

First Affiliated Hospital of Hebei North University

chenyanlinzjk@163.com+86 156 1230 3296

Outcome results

None listed

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