Clinical application of ultrasound-guided erector spinae block in posterior lumbar surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000038037

Enrollment

Unknown

Registered

2020-09-09

Start date

2020-10-01

Completion date

Unknown

Last updated

2022-06-20

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

Conditions

posterior lumbar surgery

Interventions

ESP group:erector spinae plane block, ESP

ED group:ESPB+DEX

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: After obtaining written consent from the Medical Ethics Committee of the hospital, 90 patients who underwent general anesthesia surgery within two segments of the lumbar spine, aged 18 to 70 years, BMI 20 to 27 kg / m2, American Association of Anesthesiologists (ASA) grade I to II.

Exclusion criteria

Exclusion criteria: Puncture point infection, abnormal coagulation function, local anesthetic drug allergy, severe heart and lung disease, liver and kidney insufficiency or mental illness, long-term history of taking analgesics, second operation of posterior lumbar spine.

Design outcomes

Primary

Measure	Time frame
VAS;block lever;Number of intraoperative hemodynamic instability;Intraoperative use of opioids and muscle relaxants;PCIA compression times;Number of rescue analgesics;Patient satisfaction;Nausea and vomiting;	—

Countries

China

Contacts

Public ContactLiu Jieting

Lanzhou University Second Hospital

49005110@qq.com+86 13519688766

Outcome results

None listed

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