Data CollectionNCT01600144
Data Collection for CAD Evaluation
An observational study of Data Collection, run by Universitaire Ziekenhuizen KU Leuven at 1 site in Belgium.
Trial summary
Mammographical data collection (raw data) for CAD evaluation by VUCOMp software. Read more about this study
- Who is it for?
- Any age, women only
- Conditions the study is for
- Data Collection
- What is being tested?
- digital mammography
- How many people
- 100 participants
- Where
- 1 siteBelgium
- Study dates
- Mar 2012to Aug 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- Women only
- No healthy volunteers
- Child, Adult, Older adult
Study population: women
Who may be able to join
- women who underwent a digital mammography imaging
Who cannot join
- men
Trial locations and contacts
1 site in 1 country.
Belgium1 site, 1 recruiting
- Recruiting
UZLeuven
Leuven, 3000
Hilde Vandenhoutte, PhD, (0)16343636 ext. 32, hilde.vandenhoutte@uzleuven.be
Chantal Van Ongeval, MD,Phd
About this study
Mammographical data collection (raw data) for CAD evaluation by VUCOMp software.
- Conditions
- Data Collection
- Being tested
- digital mammography
- Keywords
- data mammography
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
digital mammographyOther
data collection
| Study group | Role | What they receive |
|---|---|---|
| data collection | Not described Receives: Other: digital mammography |
What is being measured
The primary outcome is the main question the study is designed to answer.
Datacollection
No outcome described, only datacollection
Measured: 2 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 May 2012 (estimated)
- Study startMar 2012
- Primary completionAug 2025 (estimated)
- Study completionAug 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Data CollectionStudies of the same condition, open and under way.
- More trials run by Universitaire Ziekenhuizen KU LeuvenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Universitaire Ziekenhuizen KU Leuven
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Chantal Van Ongeval, MR,Phd, Principal investigator, Universitaire Ziekenhuizen KU Leuven
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01600144
- Sponsor's protocol ID
- s53792
- Status last verified
- Jul 2024
- First submitted
- 14 May 2012
- Last updated
- 3 Jul 2024
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 3 Jul 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Data Collection for CAD Evaluation
- ClinicalTrials.gov ID
- NCT01600144
- Acronym / sponsor ID
- s53792
- Conditions
- Data Collection
- Keywords
- data mammography
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Universitaire Ziekenhuizen KU LeuvenUniversity, hospital or other
- Study start
- Mar 2012 (actual)
- Primary completion
- Aug 2025 (estimated)
- Study completion
- Aug 2025 (estimated)
- First posted
- 16 May 2012 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Mammographical data collection (raw data) for CAD evaluation by VUCOMp software.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| data collection | – | Other: digital mammography |
Who may qualify
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- women
Key inclusion criteria (1 listed)
- women who underwent a digital mammography imaging
Key exclusion criteria (1 listed)
- men
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| digital mammographydata collection | Other | data collection |
Primary outcome
Datacollection
Time frame: 2 years
No outcome described, only datacollection
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Jul 2024.
Related trials for Data Collection
Recruiting
Demographic Data Collection in Healthcare
Implementation Strategies
RecruitingObservational study
Collection of Clinical Data and Specimens for Research in Hearing, Balance, Taste, Smell, Voice, Speech, and Language Disorders.
Hearing Loss, Deafness
RecruitingObservational study
The Indiana Myeloma Registry
Plasma Cell Dyscrasias
RecruitingObservational study
A Rehabilitation Data Collection Study in Patients With Spinal Cord Injury
Spinal Cord Injuries (SCI)
Not yet recruitingObservational study
A Clinical Multimodal Data Collection Study for the Development of Autonomous Ultrasound Scanning Robotic Technology
Multimodal Ultrasound Data Collection
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Chantal Van Ongeval, MR,Phd principal investigator
Universitaire Ziekenhuizen KU Leuven
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Data Collection, run by Universitaire Ziekenhuizen KU Leuven at 1 site in Belgium.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 3 Jul 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Chantal Van Ongeval, MD,Phd ((0)16343746 ext. +32, chantal.vanongeval@uzleuven.be), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Datacollection (time frame: 2 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Jul 2024.