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Efficacy of ultrasound-guided erector spinae plane block on postoperative quality of early recovery and analgesia after video-assisted thoracic surgery: a randomized controlled trial

Efficacy of ultrasound-guided erector spinae plane block on postoperative quality of early recovery and analgesia after video-assisted thoracic surgery: a randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033238
Enrollment
Unknown
Registered
2020-05-25
Start date
2020-06-01
Completion date
Unknown
Last updated
2020-05-25

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

Conditions

Lung Tumor

Interventions

experimental group:Before induction of anesthesia, 30ml 0.33% ropivacaine was used for erector spinae plane block
control group:No special treatment was given before induction of anesthesia

Sponsors

Cancer Center of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with ASAI~II, BMI18~30 kg/m2 and aged 18-65 years were selected for unilateral thoracoscopic surgery. The selected surgical types included: unilateral wedge resection of the lung, segmental resection of the lung, lobectomy of the lung

Exclusion criteria

Exclusion criteria: History of opioid addiction and long-term use of analgesic drugs, severe cardiovascular and cerebrovascular diseases, abnormal liver and kidney function, known allergy to local anesthesia, local infection at the injection site, abnormal coagulation function, refusal to be included in the group or communication disorder.

Design outcomes

Primary

MeasureTime frame
QoR-40 score of 24 hours after surgery;

Secondary

MeasureTime frame
Total amount of intraoperative remifentanil;Postoperatively, 1, 6, 12, 24, 48 hours of rest and cough visual analogue scale scores;the amount of rescue tramadol use per weight;Total effective compressions of PCA at 48 h after surgery;Postoperative incidence of nausea, vomiting and dizziness;

Countries

China

Contacts

Public ContactWenfeng Wu

Cancer Center of Guangzhou Medical University

232240886@qq.com+86 13560100230

Outcome results

None listed

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