Skip to main content
Clinical Trials/NCT02747992
NCT02747992
Completed
Not Applicable

Comparisons the Analgesia of Paravertebral Block Combined With Thoracic Wall Block Versus Paravertebral Block Alone for Modified Radical Mastectomy in Breast Cancer

Sun Yat-sen University0 sites100 target enrollmentOctober 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mastectomy, Modified Radical
Sponsor
Sun Yat-sen University
Enrollment
100
Primary Endpoint
intraoperative sedation requirement
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Previous studies have shown that PVB reduces pain and postoperative nausea and vomiting after breast cancer surgery when used in addition to general anesthesia or sedation. However, major breast cancer surgery involves areas beyond the breast tissue, such as pectoral musculature.

Registry
clinicaltrials.gov
Start Date
October 2015
End Date
February 2016
Last Updated
10 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Sun Yat-sen University
Responsible Party
Principal Investigator
Principal Investigator

Nai Liang Li

Dr

Sun Yat-sen University

Eligibility Criteria

Inclusion Criteria

  • The American Society of Anesthesiologists (ASA) Physical Status classification I to III
  • 20 - 75 years of age
  • female gender

Exclusion Criteria

  • body mass index (BMI) ≥ 35 kg/m2
  • modified radical mastectomy not performed by the single surgeon (Ben Long Yu)
  • anesthesia not performed by the single anesthesiologist (Nai Liang Li)

Outcomes

Primary Outcomes

intraoperative sedation requirement

Time Frame: during operation

target controlled infusion (TCI) propofol driven by the Schnider model in effect site control titrated to reach conscious sedation defined as Observer Assessment of Alertness/Sedation score of 2 to 3

Secondary Outcomes

  • time to first request of analgesics(postoperative 12 hours)
  • postoperative analgesic requirement(postoperation to discharge)
  • side effects(postoperation to within 24 hours after discharge)

Similar Trials