Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02085239

Comparison of Long vs. Short Acting Anesthesia for Improving Pain Management After Breast Biopsy

Comparison of Long Acting vs. Short Acting Anesthetic Agents as a Tool for Improving Pain Management Post Ultrasound Guided Breast Biopsy

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
TriHealth Inc. · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

This study will evaluate the potential role of a long acting anesthetic (ropivacaine) in providing an extended period of pain relief for patients undergoing ultrasound guided core biopsy of the breast.

Detailed description

The purpose of this study is to evaluate the potential role of a long acting anesthetic (ropivacaine) in providing an extended period of pain relief for patients undergoing ultrasound guided core biopsy of the breast. One group of patients will receive lidocaine alone for local anesthesia. A second group of patients will similarly receive lidocaine prior to tissue sampling, followed by infiltration of the biopsy area with ropivacaine. Our hypothesis is that patients who receive a long acting anesthetic (ropivacaine) along with the popular short acting anesthetic (lidocaine), will be pain free after the breast biopsy procedure for a longer period of time than the patients who only receive lidocaine (the short acting anesthetic). This will lessen the emotional and physical trauma associated with the procedure and give patients a better experience thereby improving patient care.

Conditions

Interventions

TypeNameDescription
DRUGLidocaine Ropivacaine* 8-10 ml of Lidocaine given by subcutaneous injection * 8-10 ml of Ropivacaine given by subcutaneous injection
DRUGLidocaine alone

Timeline

Start date
2013-08-01
Primary completion
2015-03-01
Completion
2015-03-01
First posted
2014-03-12
Last updated
2018-09-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02085239. Inclusion in this directory is not an endorsement.