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Intraoperative Use of the BP Device for Detecting Positive Margins During Lumpectomy Procedure

NCT00380952 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2008-05-28

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

Dune Device

Sponsors & Collaborators

  • Dune Medical Devices

    lead INDUSTRY

Principal Investigators

  • Dan Hershko, Dr. · Rambam MC

  • Rona Spector, Dr. · Rabin MC

  • Eran Sharon · Rabin MC

  • Zvi Kaufman, Dr. · Meir MC

  • Tal Kopelman, Dr. · Bnei Zion Mc

  • Yuri Berlin, Dr. · HaEmek MC

  • Moshe Papa, Prof. · Sheba Mc

  • Tanir Allweis, Dr. · Haddasah Medical Organization

  • Shlomo Schneebaum, Prof. · Souraski MC

  • Moshe Carmon, Dr. · Shaare Zedek MC

  • Amram Adari, Dr. · Ziv Mc

  • Moshe Zilberman, Dr. · Poria MC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-11-30
Primary Completion
2007-10-31
Completion
2008-04-30

Countries

  • Israel

Study Locations

More Related Trials

Entities

Diseases

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 NCT00380952 on ClinicalTrials.gov