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Ultrasound-guided Erector Spinae Plane Block Versus Caudal Block for Postoperative Analgesia in Pediatric Patients Undergoing Laparoscopic Surgery : a prospective, double-blind, randomized controlled trial

Ultrasound-guided Erector Spinae Plane Block Versus Caudal Block for Postoperative Analgesia in Pediatric Patients Undergoing Laparoscopic Surgery : a prospective, double-blind, randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078013
Enrollment
Unknown
Registered
2023-11-27
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

Postoperative pain in children

Interventions

Erector Spinae Plane Block:The child was placed in the prone position for bilateral erector spinae plane block. After disinfection of the skin with iodophor, the ultrasound probe was placed 1-2 cm lat
Caudal Block:The child was placed in the lateral decubitus position for sacral block under ultrasound guidance. After disinfection of the skin, an ultrasound probe was placed transversely over the sac

Sponsors

Peking University First Hospital Ningxia Women's and Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 7 Years

Inclusion criteria

Inclusion criteria: 1. Children aged between 1 and 7 years; 2. American Society of Anesthesiologists (ASA) grade I or II; 3. Elective laparoscopic surgery under general anesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients with spinal or spinal cord abnormalities who are not suitable for caudal block; 2. Patients with altered mental status who were not suitable for pain assessment; 3. Children with growth retardation; 4. Hematological diseases and abnormal coagulation are not suitable for caudal block; 5. Injection site infection; 6. Study drug allergy; 7. Severe liver, kidney and heart disease; 8. Parents or children refused the trial; 9. Parents or children refused to use analgesic pump after surgery.

Design outcomes

Primary

MeasureTime frame
FLACC score at 6 h after operation;

Secondary

MeasureTime frame
The time of first rescue analgesia;Postoperative adverse outcomes;Satisfaction of parents;FLACC score at 2h, 12h, 18h, and 24h after operation;the number of patient-controlled times and total sufentanil doses within 24 hours after surgery ;

Countries

China

Contacts

Public ContactQiaoli Yin

Peking University First Hospital Ningxia Women's and Children's Hospital

982426110@qq.com+86 134 6957 7852

Outcome results

None listed

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