Data Collection for CAD Evaluation
Sponsor
Universitaire Ziekenhuizen Leuven (Other)
Overall Status
Unknown status
CT.gov ID
NCT01600144
Collaborator
(none)
100
1
Study Details
Study Description
Brief Summary
Mammographical data collection (raw data) for CAD evaluation by VUCOMp software.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Study Design
Study Type:
Observational
Anticipated Enrollment
:
100 participants
Time Perspective:
Prospective
Study Start Date
:
Mar 1, 2012
Primary Completion Date
:
Aug 1, 2014
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| data collection
|
Other: digital mammography
data collection
|
Outcome Measures
Primary Outcome Measures
- Datacollection [2 years]
No outcome described, only datacollection
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
- women who underwent a digital mammography imaging
Exclusion Criteria:
- men
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | UZLeuven | Leuven | Belgium | 3000 |
Sponsors and Collaborators
- Universitaire Ziekenhuizen Leuven
Investigators
- Principal Investigator: Chantal Van Ongeval, MR,Phd, Universitaire Ziekenhuizen Leuven
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Universitaire Ziekenhuizen Leuven
ClinicalTrials.gov Identifier:
NCT01600144
Other Study ID Numbers:
- s53792
First Posted:
May 16, 2012
Last Update Posted:
Aug 7, 2014
Last Verified:
Mar 1, 2012
Keywords provided by Universitaire Ziekenhuizen Leuven