Clinical Trials Directory

Trials / Completed

CompletedNCT06427551

Volume Effect in Peng Block for Total Hip Replacement

Peng Block in Total Hip Replacement: Effects of Anesthetic Volume on Clinical Outcome and Postoperative Complications

Status
Completed
Phase
Study type
Observational
Enrollment
120 (actual)
Sponsor
Azienda Ospedaliero, Universitaria Pisana · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is to investigate whether a different volume of ropivacaine, with the same prescribed dosage based on body weight, can affect block efficacy, duration and side effects in the first 24 hours postoperatively.

Detailed description

patients were divided into 3 groups on the basis of the volume of anesthetic given to perform the block. in every patient was assessed the nrs, the side effects, if any, and the need for analgesic drugs in the first 24 hour after surgery

Conditions

Interventions

TypeNameDescription
DRUGRopivacaineThe local anesthetic was dosed on the patient's weight (50-59kg: 120mg, 60-61kg: 140mg, 70-79kg: 160mg, ≥80kg: 180mg)

Timeline

Start date
2022-01-01
Primary completion
2024-01-30
Completion
2024-01-30
First posted
2024-05-24
Last updated
2024-05-24

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT06427551. Inclusion in this directory is not an endorsement.

Volume Effect in Peng Block for Total Hip Replacement (NCT06427551) · Clinical Trials Directory