NCT01600144

Brief Summary

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

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2012

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2012

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

May 14, 2012

Completed
2 days until next milestone

First Posted

Study publicly available on registry

May 16, 2012

Completed
13.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2025

Completed
Last Updated

July 3, 2024

Status Verified

July 1, 2024

Enrollment Period

13.4 years

First QC Date

May 14, 2012

Last Update Submit

July 2, 2024

Conditions

Data Collection

Keywords

data mammography

Outcome Measures

Primary Outcomes (1)

  • Datacollection

    No outcome described, only datacollection

    2 years

Study Arms (1)

data collection

Other: digital mammography

Interventions

digital mammographyOTHER

data collection

data collection

Eligibility Criteria

Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

women

You may qualify if:

  • women who underwent a digital mammography imaging

You may not qualify if:

  • men

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UZLeuven

Leuven, 3000, Belgium

RECRUITING

Study Officials

  • Chantal Van Ongeval, MR,Phd

    Universitaire Ziekenhuizen KU Leuven

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Chantal Van Ongeval, MD,Phd

CONTACT

(0)16343746chantal.vanongeval@uzleuven.be

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 14, 2012

First Posted

May 16, 2012

Study Start

March 1, 2012

Primary Completion

August 1, 2025

Study Completion

August 1, 2025

Last Updated

July 3, 2024

Record last verified: 2024-07

Locations

BE(1)