Patients' Positions on Analgesic Efficacy of ESPB
Recruiting now · Not applicable
Conditions studied: Erector Spinae Plane Block
In brief
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
Key facts
- Study ID
- NCT06441071
- Run by
- Nanjing First Hospital, Nanjing Medical University
- People needed
- 200
- Starts
- 2024-06-14
- Expected to finish
- 2026-12-01
- Last updated by the study team
- 2025-07-21
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients undergoing Video-assisted Thoracoscopic Surgery under elective general anaesthesia were selected, regardless of sex, age 18-80 years, BMI: 18-30 kg.m-2, ASA classification I-III.
You may not qualify if…
- Allergy to the study drug or allergy to local anaesthetics;
- History of opioid abuse;
- Previous nerve block puncture with puncture site infection；
- Peripheral neuropathy；
- Coagulation abnormalities, defined as prothrombin time or partial activation time prothrombin time exceeding standard values or international normalised ratio (INR) ≥ 1.4, or platelet count ≤ 70 x 109 L-1.
Where it is running
- Nanjing First Hospital — Nanjing, Jiangsu, China (enrolling)
Full record on ClinicalTrials.gov
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