ClinicalTrials.Veeva

Menu

ESPB vs TPVB for Postoperative Analgesia After the Nuss Procedure

S

Sichuan University

Status

Completed

Conditions

Nerve Block
Analgesia
Pectus Excavatum

Treatments

Procedure: ESPB group
Procedure: TPVB group

Study type

Interventional

Funder types

Other

Identifiers

NCT05034601
2021-866

Details and patient eligibility

About

This is a prospective randomized double-blind non-inferiority trial designed to test the hypothesis that erector spinae plane block (ESPB) is non-inferior to thoracic paravertebral block (TPVB) in postoperative pain control after pectus excavatum repair.

Enrollment

68 patients

Sex

All

Ages

4 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 4 to 18 years Scheduled for elective Nuss surgery Written informed consent is obtained from parents of each patient.

Exclusion criteria

  • Coagulation dysfunction. American Society of Anesthesiologists Physical Status 4 or 5. Allergy to study medication. Local infection at the site of injection or systemic infection. Inability to understand Chinese.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

68 participants in 2 patient groups

ESPB group
Experimental group
Description:
0.25% ropivacaine 0.5 ml/kg is injected at the fascial plane deep to the erector spinae muscle
Treatment:
Procedure: ESPB group
TPVB group
Active Comparator group
Description:
0.25% ropivacaine 0.5 ml/kg is injected into the thoracic paravertebral space (T5) using TPVB approach.
Treatment:
Procedure: TPVB group

Trial contacts and locations

1

Loading...

Central trial contact

Jing Yang, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems