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Clinical Trial 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.


Clinical Trial 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 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06427551
Study type Observational
Source Azienda Ospedaliero, Universitaria Pisana
Contact
Status Completed
Phase
Start date January 1, 2022
Completion date January 30, 2024

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