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NCT02865239: EFIMED

Feasibility Study of Breast MRI in Decubitus Position

Completed NA Last updated 8 August 2018
What this trial tests

NA trial testing Position for the 3.0 Tesla in Magnetic Resonance Imaging in Breast Cancer in 15 participants. Completed in 20 August 2015.

Timeline
25 June 2015
Primary endpoint
20 August 2015
20 August 2015

Quick facts

Lead sponsorInstitut de Cancérologie de Lorraine
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designcrossover
Maskingnone
Primary purposeother
Enrollment15
Start date25 June 2015
Primary completion20 August 2015
Estimated completion20 August 2015
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Institut de Cancérologie de Lorraine — full company profile →

Who can join

Under 18, female only, with Breast Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Breast MRI is performed in prone position which causes a number of questions. Indeed, the correlation with mammography and echography and the identification of preoperative lesions can be complex as echography and surgery are carried in supine position while mammography is performed in standing position. Moreover, the prone position is often considered as uncomfortable by the patients. However, there is few publications in the literature on breast MRI in decubitus position.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Breast Cancer

Currently open trials in the same condition.

Other Institut de Cancérologie de Lorraine 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/NCT02865239.

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