Clinical Trials Directory

Trials / Completed

CompletedNCT03043755

PECS and Parasternal Block for Breast Surgery

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

Status
Completed
Phase
Study type
Observational
Enrollment
32 (actual)
Sponsor
Istituti Ospitalieri di Cremona · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2016-07-01
Primary completion
2016-12-01
Completion
2017-02-01
First posted
2017-02-06
Last updated
2017-02-06

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT03043755. Inclusion in this directory is not an endorsement.