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PECS and Parasternal Block for Breast Surgery — PARAST  

Mastectomy Clinical Trial

Official title:
Observational Study to Evaluated Efficacy of Parasternal and PECS Blocks Association in Breast Surgery

Clinical Trial Summary

Propose to evaluate efficacy of association between US guide parasternal block and pectorals nerves block (PECS) as anesthetic option for breast surgery (medial quadrantectomy and simple mastectomy).

All patients undergoing medial quadrantectomy and simple mastectomy in 6 months period will be observed.

All patients receive: US guide parasternal block at T4 and T6 space with 6ml of ropivacaine 0,75% and PECS type 2 block performed with 24ml of ropivacaine 0,75%.

During surgery patients receive light sedation with continuous infusion of propofol

Will be observed:

Additional local anesthetic infiltration from surgeon. Pain at rest and during movement quantified as Numerical Rating Scores (0-10) during the first 12 hours postoperatively.

Eventual side effects such as nausea/vomiting.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03043755
Study type Observational
Source Istituti Ospitalieri di Cremona
Contact
Status Completed
Phase N/A
Start date July 2016
Completion date February 2017
View Details
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