Trials / Completed
CompletedNCT00380952
Intraoperative Use of the BP Device for Detecting Positive Margins During Lumpectomy Procedure
MAST Study Protocol
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 300 (actual)
- Sponsor
- Dune Medical Devices · Industry
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This protocol was designed for testing the intraoperative use of the Dune device. This multicenter study will take place in Israel at 12 sites.
Detailed description
Use of the device will take place during a partial mastectomy procedure (lumpectomy).The patient will be randomized to enter the device or control arm.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Dune Device |
Timeline
- Start date
- 2006-11-01
- Primary completion
- 2007-10-01
- Completion
- 2008-04-01
- First posted
- 2006-09-27
- Last updated
- 2008-05-28
Locations
9 sites across 1 country: Israel
Source: ClinicalTrials.gov record NCT00380952. Inclusion in this directory is not an endorsement.