Clinical trial · Interventional
Early Detection of Breast Cancer Using Tomosynthesis Imaging
NCT00637598CI-TRIAL-00026981completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose is to develop digital tomosynthesis to improve the detection of breast cancers. The aims are optimizing digital mammography and tomosynthesis acquisition, creating visualization tools, prospective pilot studies to evaluate radiologist performance, and computer-aided detection.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Neoplasms | Breast Neoplasm | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Mammography and tomosynthesis imaging | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Tomosynthesis scans
- description
- This is a case-only study with only one group/cohort. All women receive both mammography and tomosynthesis imaging.
- interventionNames
- Radiation: Mammography and tomosynthesis imaging
Primary outcomes (1)
- measure
- Radiologist ROC (receiver operating characteristic) area under curve (AUC)
- timeFrame
- at imaging review by the end of the study, approximately 9 years
Eligibility
Eligibility (as posted)
- Sex
- Female
Show eligibility criteria text
Inclusion Criteria: All Subjects accepted for this clinical study must: * Be already scheduled to undergo screening mammography, diagnostic mammography, or breast biopsy for standard clinical indications * Provide written informed consent * Be able to communicate effectively with clinical study personnel. Exclusion Criteria: Subjects with any of the following conditions will be excluded from this clinical study: * Childbearing potential and subject refuses serum pregnancy test or test result is positive.
References
Publications (0)
Data not yet available
No reference posted for this study.