American Breast Laser Ablation Therapy Evaluation
Status: | Recruiting |
---|---|
Conditions: | Breast Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/16/2019 |
Start Date: | December 2008 |
End Date: | June 2020 |
Contact: | Marti DeLay |
Email: | info@novianhealth.com |
Phone: | 312-266-7200 |
American Breast Laser Ablation Therapy Evaluation (ABLATE): Monitoring the Long Term Safety and Efficacy of Novilase™ Breast Interstitial Laser Therapy in Real World Application
The purpose of this patient tracking program is to monitor long term safety and effectiveness
of the Novilase™ device and method in real world application.
of the Novilase™ device and method in real world application.
ABLATE is a prospective, observational multi-center tracking database which will evaluate
clinical outcomes from patients undergoing Novilase for benign breast conditions (i.e.
fibroadenomas, papillomas, etc). Data captured will assess the potential advantages and
disadvantages of the procedure as compared with lumpectomy. Tumor characteristics, equipment
used, complications, patient satisfaction and cosmesis ratings will also be tracked.
clinical outcomes from patients undergoing Novilase for benign breast conditions (i.e.
fibroadenomas, papillomas, etc). Data captured will assess the potential advantages and
disadvantages of the procedure as compared with lumpectomy. Tumor characteristics, equipment
used, complications, patient satisfaction and cosmesis ratings will also be tracked.
Inclusion Criteria:
- Diagnosis confirmed by needle core biopsy
- Tumors detected either by physical exam or imaging
- Tumors do not exceed 2 cm in diameter and measure at least 0.5 cm away from the skin
and chest wall
- Single, multiple and/or bilateral tumors
- Patient has given consent prior to being treated with Novilase™
Exclusion Criteria:
- Patient is pregnant or lactating
- Hypercellularity suggestive of phyllodes
- Atypia
- Equivocal pathology report (e.g., discordance between radiographic and microscopic
results)
- Fibroadenomas with stromal solidarity
We found this trial at
1
site
177 Fort Washington Avenue
New York, New York 10032
New York, New York 10032
Principal Investigator: Margaret Chen, M.D.
Phone: 212-305-9676
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