Patients' Positions on Analgesic Efficacy of ESPB

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorNanjing First Hospital, Nanjing Medical University

About this trial

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

Eligibility criteria

Qualifiers

None

Disqualifiers

Allergy to the study drug or allergy to local anaesthetics;

History of opioid abuse;

Previous nerve block puncture with puncture site infection;

Peripheral neuropathy;

Trial design

Treatments tested in this trial

  • position

Treatment groups

200 Participants
are divided into 4 treatment groups