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Efficacy of Pectoral Nerve Block for Breast Reduction Surgery

NCT03857386 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 53

Last updated 2019-04-30

No results posted yet for this study

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.

Conditions

  • Nerve Blocks
  • Breast Surgery
  • Postoperative Pain

Interventions

PROCEDURE

PECS group

Pecs block performed using ultrasound guidance

PROCEDURE

Control group

Local infiltration anesthesia performed during the operation

Sponsors & Collaborators

  • Antalya Training and Research Hospital

    lead OTHER_GOV

Principal Investigators

  • Arzu Karaveli · Netherlands: Ministry of Health, Welfare and Sports

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-07-01
Primary Completion
2018-03-01
Completion
2018-05-01

Countries

  • Turkey (Türkiye)

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 NCT03857386 on ClinicalTrials.gov