A randomised trial for erector spinae plane block for analgesia after video-assisted thoracoscopic surgery children

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000031763

Enrollment

Unknown

Registered

2020-04-09

Start date

2020-05-01

Completion date

Unknown

Last updated

2020-04-13

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

Conditions

Postoperative pain

Interventions

Control group:intravenous analgesia

experimental group:ESPB: 0.2% Ropivacaine 1.5 mg/kg

Eligibility

Sex/Gender

All

Age

No minimum to 6 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade I-III; 2. Aged 0-6years; 3. Schedualed for unilateral thoracoscopic surgery.

Exclusion criteria

Exclusion criteria: 1. Coagulation dysfunction, severe spinal deformity or suspected ultrasound anatomical abnormality; 2. Requiring re-exploration, and requiring redo or emergency surgery; 3. Local anesthetic hypersensitivity; 4. Requiring intubation for more than 3 hours; 5. Gestational age less than 32 weeks; 6. Preoperative diagnosis of hypoxic ischemic encephalopathy.

Design outcomes

Primary

Measure	Time frame
FLACC ??;Analgesic rescue;	—

Secondary

Measure	Time frame
heart rate response to incision;	—

Countries

China

Contacts

Public ContactLi Ma

7th Medical Center of the Chinese PLA General Hospital

acellor@163.com+86 13426324875

Outcome results

None listed

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