Clinical study of ultrasound-guided single erector spinae plane block for analgesia in thoracoscopic lobectomy

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000034437

Enrollment

Unknown

Registered

2020-07-05

Start date

2018-03-01

Completion date

Unknown

Last updated

2020-07-06

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

Conditions

Erector spinae plane block for analgesia

Interventions

Experimental group:ultrasound-guided single erector spinae plane (ESP) block

control group:ultrasound-guided single erector spinae plane (ESP) block

Eligibility

Sex/Gender

All

Age

40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. ASA physical status I–II; 2. aged 40-70 years; 3. scheduled for elective video-assisted thoracoscopic assisting small incision lobectomy.

Exclusion criteria

Exclusion criteria: 1. obesity (body mass index > 35kg/m2); 2. known allergy to study drugs; 3. skin infection at the site of the needle puncture; 4. coagulopathy; 5. long-term use of opioids.

Design outcomes

Primary

Measure	Time frame
NRS score postoperation;dosage of anesthetic intra-operation;complications;postoperative analgesia satisfaction of patients;	—

Countries

China

Contacts

Public ContactYuanchao Gao

Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University,

gyc242@126.com+86 18310158399

Outcome results

None listed

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