Skip to main content
Clinical Trials/NCT04036370
NCT04036370
Completed
Not Applicable

The Effect of Continuous Pectoral Nerve Block on Postoperative Analgesia Consumption in Breast Cancer Surgery

Antalya Training and Research Hospital1 site in 1 country48 target enrollmentJuly 30, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nerve Blocks
Sponsor
Antalya Training and Research Hospital
Enrollment
48
Locations
1
Primary Endpoint
analgesia consumption
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of the study is to evaluate the effect of continuous pectoral nerve block on postoperative analgesia consumption in breast cancer surgery.

Detailed Description

Pectoral nerve 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 in breast cancer surgery.

Registry
clinicaltrials.gov
Start Date
July 30, 2019
End Date
November 15, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

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

Arzu Karaveli

University of Health Sciences Antalya Training and Research Hospital

Antalya Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiology (ASA) I-II
  • 18-65 years
  • Body mass index (BMI) ≤40 kg/m2
  • Elective breast cancer surgery

Exclusion Criteria

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

Outcomes

Primary Outcomes

analgesia consumption

Time Frame: 12 hours

postoperative 12 hours

Secondary Outcomes

  • analgesia consumption(during the surgery)
  • postoperative Numeric Rating Scale (NRS) score(0, 1, 3, 6, 9, 12 hours)

Study Sites (1)

Loading locations...

Similar Trials