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PECS Block in Breast Surgery: an Observational Multicenter Study

NCT02414256 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 250

Last updated 2017-01-30

No results posted yet for this study

Summary

We will enroll patients submitted to breast surgery (in and outsettings) with regional anesthesia.

The blinded observers, in the first 48 hours post-operative, will evaluate (telephone interview in outsetting) the pain intensity through the Numeric Rating Scale ( 0= no pain, 10 = worst possible pain) thereby recording the treatment procedures in accordance with usual clinical practice. At the same time we will evaluate the presence of intraoperative or postoperative complications related to regional anesthesia, the PONV rate (post-operative nausea and vomiting) and the analgesic/antiemetic therapy.

Conditions

  • Postoperative Pain

Interventions

OTHER

regional anesthesia in breast surgery

In the Hospitals involved in this study are performed routinely wall blocks (PECS I-II blocks and serratus block) during breast surgery

Sponsors & Collaborators

  • Ospedale di Circolo - Fondazione Macchi

    lead OTHER

Principal Investigators

  • Andrea L Ambrosoli, MD · University Hospital Varese

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2015-04-30
Completion
2016-06-30

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02414256 on ClinicalTrials.gov