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Quality Study of Anesthetic Technique on Breast Cancer Surgery

NCT01499836 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 101

Last updated 2014-01-16

No results posted yet for this study

Summary

Previous studies have shown that paravertebral block (PVB) has the potential to reduce pain and side effects after breast surgery when used in addition to general anesthesia or sedation.The investigators would like to further discern the impact of GA or PVB on the postoperative QoR, pain and satisfaction.

Conditions

  • Postoperative Pain
  • Quality of Recovery
  • Satisfaction

Interventions

OTHER

PVB

paravertebral block

Sponsors & Collaborators

  • Nai Liang Li

    lead OTHER

Principal Investigators

  • Nai Liang Li · Koo Foundation Sun Yat-Sen Cancer Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2013-04-30
Completion
2013-06-30

Countries

  • Taiwan

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 NCT01499836 on ClinicalTrials.gov