Data Collection for CAD Evaluation

Data Collection Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01600144
• Other study ID #: s53792
• Status: Recruiting
• Phase: N/A
• First received: May 14, 2012
• Last updated: August 6, 2014
• Start date: March 2012

Study information

• Verified date: March 2012
• Source: Universitaire Ziekenhuizen Leuven
• Contact: Chantal Van Ongeval, MD,Phd
• Phone: (0)16343746
• Email: chantal.vanongeval[@]uzleuven.be
• Is FDA regulated: No
• Health authority: Belgium: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

Mammographical data collection (raw data) for CAD evaluation by VUCOMp software.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. primary completion date: August 2014
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• women who underwent a digital mammography imaging

Exclusion Criteria:

• men

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

• Data Collection

Intervention

Other:
• digital mammography
data collection

Locations

Country	Name	City	State
Belgium	UZLeuven	Leuven

Sponsors (1)

Lead Sponsor	Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Datacollection	No outcome described, only datacollection	2 years	No