Clinical Trials Directory

Trials / Completed

CompletedNCT04306133

PENG Block Combined to Wound Infiltration for Hip Replacement

Pericapsular Nerve Group (PENG) Block Combined to Wound Infiltration vs. Wound Infiltration Alone for Postoperative Analgesia After Total Hip Replacement: a Prospective Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Campus Bio-Medico University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study analyze the effect of Pericapsular Nerve Group (PENG) Block combined to wound infiltration for analgesia after elective hip replacement. Half of participants will receive a PENG Block combined with wound infiltration, while the other half will receive wound infiltration alone.

Conditions

Interventions

TypeNameDescription
PROCEDUREPENG blockAfter performing spinal anesthesia, PENG block with 20 mL of 0.375 % Ropivacaine will be executed as described by Giron-Arongo et al with a low frequency curvilinear probe. A 22G 80 mm needle (Stimuplex Ultra 360, Braun ) will be used.
PROCEDUREWound InfiltrationAt the end of operation, the surgeon will perform wound infiltration with 20 mL of 0.375 % Ropivacaine.

Timeline

Start date
2020-03-09
Primary completion
2020-12-24
Completion
2020-12-31
First posted
2020-03-12
Last updated
2021-04-06

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT04306133. Inclusion in this directory is not an endorsement.