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NCT03520127

A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast Lesion Excision System (BLES)

Terminated Last updated 16 May 2019
What this trial tests

trial testing Intact Breast Lesion Excision System (BLES) in Breast Lesions in 176 participants. Terminated before completion.

Timeline
27 September 2017
Primary endpoint
15 February 2019
28 February 2019

Quick facts

Lead sponsorMedtronic Surgical Technologies
StatusTerminated
Study typeOBSERVATIONAL
Enrollment176
Start date27 September 2017
Primary completion15 February 2019
Estimated completion28 February 2019
Sites7 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Medtronic Surgical Technologies

Who can join

18 and older, female only, with Breast Lesions. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this registry study is to collect use and clinical outcomes data following breast lesion excision or sampling with the Intact BLES.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Medtronic Surgical Technologies trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03520127.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing