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Clinical Trials/NCT03857386
NCT03857386
Completed
Not Applicable

Comparison of The Effects of Pectoral Nerve Block and Local Infiltration Anesthesia on Postoperative Analgesia for Breast Reduction Surgery

Antalya Training and Research Hospital1 site in 1 country53 target enrollmentJuly 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nerve Blocks
Sponsor
Antalya Training and Research Hospital
Enrollment
53
Locations
1
Primary Endpoint
postoperative visual analog scale (VAS) score
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of the study is to evaluate the efficacy of PECS block applied to patients undergoing bilateral breast reduction surgery on postoperative analgesia compared to local infiltration anesthesia.

Detailed Description

Pectoral nerve block (PECS block) has been developed as an alternative to thoracic paravertebral and/or thoracic epidural blocks in recent years. It is frequently applied for postoperative analgesia especially in breast cancer surgery and subpectoral breast prosthesis.

Registry
clinicaltrials.gov
Start Date
July 1, 2017
End Date
May 1, 2018
Last Updated
7 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Antalya Training and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Arzu Karaveli

study director

Antalya Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiology (ASA) I-II
  • body mass index (BMI) ≤40 kg/m2
  • elective bilateral breast reduction surgery

Exclusion Criteria

  • declining to give written informed consent
  • ASA III and above
  • under 18 years of age or over 65 years of age
  • history of allergy against to the local anesthetics,
  • controendication of peripheral block or local anesthetic infiltration (local infection, coagulopathy, etc.)
  • history of breast surgery
  • treatment due to psychiatric disorder
  • history of treatment for a chronic pain
  • history of nerve blocks in order to treat postoperative pain

Outcomes

Primary Outcomes

postoperative visual analog scale (VAS) score

Time Frame: postoperative 0, 1, 3, 6, 9, and 12 hours

Postoperative pain assessment will be performed using the VAS score (VAS 0 = no pain, VAS 10 = most severe pain possible). The VAS scores will be recorded at postoperative 0, 1, 3, 6, 9, and 12 hours.

Secondary Outcomes

  • analgesia consumption(during the surgery)
  • length of hospital(4 days)

Study Sites (1)

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