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Sonography-guided Pericapsular Never Group Block for Hip Arthroplasty — QUASH  

Analgesia Clinical Trial

Official title:
Sonography-guided Pericapsular Nerve Group Block for Hip Arthroplasty

Clinical Trial Summary

In this study, the investigator will examine the efficacy of Pericapsular nerve group (PENG) block in hip arthroplasty as a post-operative pain management technique, study the analgesia, opioid-sparing effects and motor-blocking effects of the PENG block

Clinical Trial Description

PENG Block group (PG) will receive 0.5%Ropivacaine in 20 ml of saline. Sham Block group (SG) will receive 20 ml of saline Patient will be sedated with IV midazolam before nerve block. After peripheral nerve block ,general anesthesia will be conducted using sufentanyl, propofol and rocuronium for induction and propofol and sevoflurane for maintenance. Tests will be operated after procedureļ¼Œand recorded up to 48 hours after surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04480320
Study type Interventional
Source Guangzhou First People's Hospital
Contact
Status Recruiting
Phase N/A
Start date September 10, 2020
Completion date March 31, 2021
View Details
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