Feasibility Study of Supine Breast MRI : Comparison With Prone MRI and Comfort Assessment

Breast Diseases Clinical Trial

Official title:

Feasibility Study of Supine Breast MRI : Comparison With Prone MRI and Comfort Assessment

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03088436
• Other study ID #: ICL_2014_0003
• Status: Completed
• Phase: N/A
• First received: March 17, 2017
• Last updated: March 17, 2017
• Start date: January 1, 2014
• Est. completion date: January 15, 2015

Study information

• Verified date: March 2017
• Source: Institut de Cancérologie de Lorraine
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The aim of the present study was to determine the prone-to-supine displacement of breast lesions using preoperative prone MRI and supine second-look ultrasound data

Recruitment information / eligibility

• Status: Completed
• Enrollment: 47
• Est. completion date: January 15, 2015
• Est. primary completion date: January 15, 2015
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• The inclusion criteria were being a woman with breast lesions whose assessment involved breast MRI and ultrasound at our institution. There were no exclusion criteria.

Exclusion Criteria:

Related Conditions & MeSH terms

• Breast Diseases

Intervention

Device:
• preoperative prone MRI and supine second-look ultrasound data
Patients were examined using a standard clinical MRI protocol in the prone position with both arms placed above the head. Second-look ultrasonographies were performed. Patients were instructed to lie supine, with their hands behind their heads.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Institut de Cancérologie de Lorraine

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	distance to the nipple (mm)	the distance to the nipple for lesion was determined using prone MRI and supine ultrasound	1 day