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.