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Effect of esketamine combined with erector spinae plane block on postoperative pain and immune function in patients underwent video-assisted thoracoscopic lobectomy

Effect of esketamine combined with erector spinae plane block on postoperative pain and immune function in patients underwent video-assisted thoracoscopic lobectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065717
Enrollment
Unknown
Registered
2022-11-13
Start date
2022-12-01
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

None listed

Interventions

Group A:Esketamine+ erector spinae plane block
Group B:Placebo+ erector spinae plane block
Group C:Simple general anesthesia

Sponsors

Ya'an People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective unilateral thoracoscopic lobectomy; 2. Aged range from 18 to 65 years, no gender limit; 3. Body mass index (BMI) 18.5 ~ 24kg/m^2; 4. ASA grading ? ~ ?.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of alcohol and drug abuse, chronic pain and neuropathy; 2. Patients with diabetes who are allergic to esketamine and ropivacaine, have coagulation dysfunction, infected at the injection site, or have poor blood sugar control; 3. Patients with liver and kidney dysfunction; 4. Patients with mental illness who cannot cooperate and communicate with others; 5. Any of the following contraindications exist in the use of Esketamine injection: (patients with serious risk of elevated blood pressure or intracranial pressure; Patients with intraocular hypertension, glaucoma or penetrating ocular trauma; Patients with poorly controlled or untreated hypertension and resting systolic/diastolic blood pressure exceeding 180/110mmHg; Patients with untreated or undertreated hyperthyroidism); 6. The patient refuses to participate.

Design outcomes

Primary

MeasureTime frame
Numeric Rating Scale (NRS) score for pain;

Secondary

MeasureTime frame
Numeric Rating Scale (NRS) score for pain;Numeric Rating Scale (NRS) score of incision pain;Remifentanil dosage;PCIA pressing times, dosage;Chronic pain occurrence;Times of remedial analgesia;Rating of chronic pain impact on life;Level of chronic pain management measures;Patient satisfaction with postoperative pain management;Level of natural killer cells (%);Level of CD4+T cells (%);Level of CD8+T cells (%);Hypotension;Hypertension;Tachycardia;Bradycardia;Use of vasopressors;Use of atropine;Nausea and vomiting;Adverse events (Respiratory depression, dizziness and mental side effects);Postoperative pulmonary complications (Respiratory tract infection, respiratory failure, pleural effusion, atelectasis, pneumothorax or bronchospasm);

Countries

China

Contacts

Public ContactZhou Shuzhi

Ya'an People's Hospital

893915648@qq.com+86 18283560691

Outcome results

None listed

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