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Effect of erector spinae plane block and perioperative intravenous infusion of lidocaine on the quality of recovery after thoracic surgery

Effect of erector spinae plane block and perioperative intravenous infusion of lidocaine on the quality of recovery after thoracic surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061778
Enrollment
Unknown
Registered
2022-07-02
Start date
2022-06-20
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

thoracic surgery

Interventions

erector spinae plane block group:Half an hour before anesthesia induction, vertical spinal muscle block was performed in a flat T5 plane with an injection dose of 0.5% ropivacaine 20 ml + betamethason
Lidocaine group:Lidocaine was pumped at 1.5mg / kg IV before anesthesia induction, followed by a rate of 1.5mg / kg / h until the end of the procedure
Saline control group:The saline control group used the same intravenous lidocaine group, and the saline erector spinae plane block group

Sponsors

The Affiliated Huai'an Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. thoracic surgery under general anesthesia (including thoracoscopic alveolectomy, mediastinal tumor resection, lobectomy, and radical lung cancer); 2. ASA I~II; 3. age 18~65 years;

Exclusion criteria

Exclusion criteria: 1. abnormal heart, lung, liver, kidney and coagulation function (including unstable ischemic heart disease; arrhythmia; complete bundle branch block; prolonged QT interval; heart failure, etc.); 2. proposed to block area infection, Severe nerve injury to the block side limb; 3. had a history of chronic pain analgesic medication, psychiatric medication, chemoradiotherapy, Patients with contraindications to non-steroidal anti-inflammatory drugs; 4. repeats or planned reoperation within 30 days of surgery; 5. to patients with allergies to local anesthetics such as lidocaine, ropivacaine, and general anesthetic drugs; 6. serum potassium abnormalities; 7. patients and family members refused surgical anesthesia and those unable to complete the questionnaire.

Design outcomes

Primary

MeasureTime frame
Quality of recovery-40 scale;Self-Rating Anxiety Scale;Self-Rating Depression Scale;Visual analogue scale;

Countries

china

Contacts

Public ContactChenglan Xie

The Affiliated Huai'an Hospital of Xuzhou Medical University

xiechenglan@163.com+86 13776701556

Outcome results

None listed

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