Effect of ultrasound-guided erector spinae plane block for postoperative analgesia after uniportal VATS

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900022217

Enrollment

Unknown

Registered

2019-03-30

Start date

2019-06-01

Completion date

Unknown

Last updated

2020-03-16

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

Conditions

postoperative pain

Interventions

Group 1:erector spinae plane block beforeVATS partial lung resection

Group 2:no block

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Aged 18-75 years old; ASA grade I-II; VATS Partial lung resection;Patients who agreed to participate in this study and signed informed consent for anesthesia.

Exclusion criteria

Exclusion criteria: refusal of ESP blockade; severe cardiovascular diseases,EF<40%; severe pulmonary diseases (FEV1/FVC<40%); liver and kidney dysfunction; chronic cough and phlegm such as chronic bronchitis and COPD; chronic pain; puncture point infections; refusal to participate in this study

Design outcomes

Primary

Measure	Time frame
Postoperative sufentanil consumption;	—

Secondary

Measure	Time frame
Postoperative first out-of-bed activity time;Postoperative hospital stay;Plasma levels of TNF, IL-6 and IL-10;Intraoperative opioid dosage;Postoperative pain score;	—

Countries

China

Contacts

Public ContactLin Liu

The Second Affiliated Hospital of Soochow University

liulinsz2015@163.com+86 18115563034

Outcome results

None listed

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