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NCT00722059 · ClinicalTrials.gov registry record · Early Phase 1
Detection and/or Evaluation of Dense Breast Abnormalities Using Tomosynthesis and Digital Mammography
A Early Phase 1 study, sponsored by University of Michigan.
- Completed
- Registry status
- Early Phase 1
- Development phase
- 50
- Enrollment target
NCT00722059: Completed Early Phase 1 study, sponsored by University of Michigan.
NCT00722059 is a Early Phase 1 study that has completed, run by University of Michigan. The registered enrollment target is 50 participants, roughly in line with the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00722059, a Early Phase 1 study, has completed, sponsored by University of Michigan.
- COMPLETED
- Registry status
- Early Phase 1
- Development phase
- 50 participants
- Enrollment target
Study Summary
The purpose of this study is to compare 3D mammography with digital mammography in women with dense breasts for the detection and evaluation of masses and/or breast cancer.
Primary Outcome
Interest of sensitivity, specificity and area under region of concern curve for malignant mass detection. During review, the number of masses and location and size of each mass will be recorded. An additional estimate of probability of malignancy will be recorded for each image sets.
Interventions
- PROCEDURE Breast Tomosynthesis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2006-04 |
| Est. Completion | 2013-10 |
| Phase | Early Phase 1 |
What the finished NCT00722059 record still lists
NCT00722059 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, roughly in line with the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 1 intervention - of which Breast Tomosynthesis is the first listed.
NCT00722059 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00722059 about?
NCT00722059 is a clinical study titled "Detection and/or Evaluation of Dense Breast Abnormalities Using Tomosynthesis and Digital Mammography". The purpose of this study is to compare 3D mammography with digital mammography in women with dense breasts for the detection and evaluation of masses and/or breast cancer.
What is the current status of trial NCT00722059?
This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 50 participants. The study started on 2006-04. Estimated completion is 2013-10.
What interventions are being tested in trial NCT00722059?
The interventions under investigation include: Breast Tomosynthesis (PROCEDURE).
Who is sponsoring clinical trial NCT00722059?
This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00722059's enrollment target sits among peer trials
50 493rd of 2000 higher than 1,468 of 2,000 other Early Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Early Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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