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Study identifier: NCT06441071 Synced from ClinicalTrials.gov · July 29, 2026
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Patients' Positions on Analgesic Efficacy of ESPB

Condition: Erector Spinae Plane Block  ·  Sponsor: Nanjing First Hospital, Nanjing Medical University

PhaseNA
Planned participants200
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn if patients remaining different positions for 30min after receiving ultrasound-guided erector spinae plane block influenced the postoperative analgesia. The main questions it aims to answer are: Does patients maintain prone position or lateral position for 30 min after ESPB provided superior analgesic effect than in the supine position? Is ESPB not inferior to PVB considering postoperative opioid consumption ? Researchers will compare the opioid consumption 24h postoperatively among the patients remaining supine, lateral, prone position after ESPB and PVB to see if patients maintaining lateral or prone position provided excellent postoperative analgesia. Participants will: Maintaining supine lateral or prone position for 30 min following ESPB or receiving PVB. Receiving postoperative NRS and QoR assessment

This description comes directly from the study's public registry record.

Talk to the study team

Xinyi Bu, MD  ·  +86 18360868010  ·  1037031075@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

Nanjing First HospitalNanjing, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06441071