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Completed No phase listed Observational Accepts healthy volunteers

Percutaneous Excision Trial

ClinicalTrials.gov ID: NCT00720642

Public ClinicalTrials.gov record NCT00720642. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 25, 2026, 8:25 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Percutaneous Excision Trial (I-Pet): A Multi-Center Clinical Study Of The Intact Breast Lesion Excision System (Bles) To Demonstrate That A Definitive Diagnosis Can Be Made From The Tissue Sample Collected With The Intact Bles.

Study identification

NCT ID
NCT00720642
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Intact Medical Corporation
Industry
Enrollment
1,170 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2006
Primary completion
May 31, 2011
Completion
May 31, 2011
Last update posted
Sep 11, 2012

2006 – 2011

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
23
Facility City State ZIP Site status
University of Arkansas for Medical Services Little Rock Arkansas 72205
The Breast Health Center Indio California 92201
Long Beach Memorial Breast Center Long Beach California 90806
The Hill Breast Center Pasadena California 91105
Flagler Hospital Saint Augustine Florida 32086
Center for Breast Care HCA West Palm Beach Florida 33407
Metro Surgical Associates, Inc. Lithonia Georgia 30058
TIFT Regionald Medical Center Tifton Georgia 31793
Maui Medical Group Wailuku Hawaii 96793
Shawnee Mission Medical Center Overland Park Kansas 66204
St. Joseph Medical Center Towson Maryland 21204
Mercy Medical Center Springfield Massachusetts 01102
Genesys Medical Center Grand Blanc Michigan 48439
Saint Luke's Cancer Institute Kansas City Missouri 64111
Lourdes Hospital Breast Center Binghamton New York 13905
Wilson Hospital Breast Center Johnson City New York 13790
Jewish Hospital Breast Center Cincinnati Ohio 45236
University of Cincinnati The Barrett Center Cincinnati Ohio 45267-0772
Elyria Memorial Hospital Elyria Ohio 44035
St. John West Shore Hospital Westlake Ohio 44145
Evangelical Hospital Lewisburg Pennsylvania 17837
Allegheny General Hospital Pittsburgh Pennsylvania 15212
Coastal Carolina Breast Center Murrells Inlet South Carolina 29576
Nashville Breast Center Nashville Tennessee 37205

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00720642, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 11, 2012 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00720642 live on ClinicalTrials.gov.

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