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OpenTrials
Completed

NCT Number: NCT02414256

PECS Block in Breast Surgery: an Observational Multicenter Study

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.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Day Surgery Ospedale di Circolo Varese

Varese, VA, 21100, Italy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

regional anesthesia in breast surgery

Other

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

Primary outcomes

  1. Pain Intensity Misure

    Time frame: 2 days

Secondary outcomes

  1. Complications Regional Anesthesia Related

    Time frame: 1 days

  2. PostOperative Nausea Rate

    Time frame: 2 days

  3. Intraoperative Opioids Use

    Time frame: surgical time

  4. Postoperative Analgesics

    Time frame: 2 days

Sponsors and collaborators

Lead sponsor

Ospedale di Circolo - Fondazione Macchi

Other

Registry information

Important dates

Study start
2015
Primary completion
2015
Study completion
2016
First posted
Apr 10, 2015
Registry last updated
Jan 30, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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