Trials / Withdrawn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- Withdrawn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
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine Ropivacaine | * 8-10 ml of Lidocaine given by subcutaneous injection * 8-10 ml of Ropivacaine given by subcutaneous injection |
| DRUG | Lidocaine 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.