Erector Spinae Plane Block v.s Patient Controlled Analgesia in Correction Surgery for Idiopathic Scoliosis

NANot yet recruitingINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

January 1, 2025

Primary Completion Date

December 31, 2026

Study Completion Date

May 31, 2027

Conditions
Idiopathic ScoliosisErector Spinae Plane BlockPatient Controlled Analgesia
Interventions
OTHER

ESPB

Participants will receive ultrasound-guided ESPB preoperatively, using 40 ml of 0.3% ropivacaine.

DEVICE

PCA

Participants will receive postoperative PCA with a formulation of 200 µg sufentanil diluted to 100 ml. The PCA settings will include a background dose of 3 ml/hour, a lockout time of 15 minutes, and a bolus dose of 2 ml.

Trial Locations (1)

610041

West China Hospital, Sichuan University, Chengdu

All Listed Sponsors
lead

West China Hospital

OTHER

NCT06728046 - Erector Spinae Plane Block v.s Patient Controlled Analgesia in Correction Surgery for Idiopathic Scoliosis | Biotech Hunter | Biotech Hunter