Clinical trial · Interventional
Breast Cancer Detection: Comparison of Breast Tomosynthesis and Conventional Mammography
NCT01669148CI-TRIAL-00028131completedN/AResults postedClinicalTrials.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 primary hypothesis to be tested is: The detection of breast cancer will be increased with tomosynthesis (3D) imaging
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 Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Conventional | Device | — | UNRESOLVED |
| Tomosynthesis | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Conventional + Tomosynthesis
- description
- conventional (2D) imaging plus tomosynthesis (3D) imaging first then tomosynthesis alone 1 month later.
- interventionNames
- Device: Tomosynthesis
- Device: Conventional
- type
- ACTIVE_COMPARATOR
- label
- Tomosynthesis alone
- description
- tomosynthesis (3D) imaging alone first then conventional (2D) imaging plus tomosyntheis 1 month later.
- interventionNames
- Device: Tomosynthesis
Primary outcomes (1)
- measure
- Detection of Breast Cancer (Sensitivity)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 35 Years
Show eligibility criteria text
Inclusion Criteria: * Female * Any ethnic origin * No contraindication for routine bilateral mammography Exclusion Criteria: Potential subjects with any of the following will not be enrolled in the study: * Any contraindications to mammographic screening, including, but not limited to: * Significant existing breast trauma * Under the age of 30 at the time of consent * Breast Implants * Prior Surgeries * Unable to understand and execute written informed consent * Pregnant * Lactating
References
Publications (0)
Data not yet available
No reference posted for this study.