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PECS Block in Breast Surgery: an Observational Multicenter Study

O

Ospedale di Circolo - Fondazione Macchi

Status

Completed

Conditions

Postoperative Pain

Treatments

Other: regional anesthesia in breast surgery

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

250 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

ASA I-II-III Patients Written Informed Consent

Exclusion criteria

ASA IV Active Heart Failure Coagulation Disease Chronic Pain Allergies to Local Anesthetics

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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