Clinical trial · Interventional
Molecular Imaging of Breast Cancer With Breast PET/CT
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Low enrollment
Summary
Brief summary (as posted)
This study is a feasibility study to determine if a combined breast PET/CT scanner can image malignant functional activity while determining anatomical structure in the same clinical setting for patients with breast cancer. End-points of this study are whether women will accept the imaging position and timing, and whether functional properties of breast cancer can be imaged with this device. The secondary purpose of this study is to explore protocol parameters with a view to optimizing imaging performance whilst minimizing patient discomfort. Imaging results will be compared to histological samples to determine ground truth.
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 (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Positron emission tomography and computed tomography | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- OTHER
- label
- 1
- description
- Normal volunteers
- interventionNames
- Radiation: Positron emission tomography and computed tomography
- type
- ACTIVE_COMPARATOR
- label
- 2
- description
- Breast PET/CT scan
- interventionNames
- Radiation: Positron emission tomography and computed tomography
- type
- ACTIVE_COMPARATOR
- label
- 3
- description
- Whole body and breast PET/CT
- interventionNames
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: \- Normal Adult Volunteers * Female, at least 18 years of age * Ability to lie motionless for up to 20 minutes Patient Volunteers * Female, at least 18 years of age * Diagnostic findings from prior mammography highly suggestive of invasive breast carcinoma (BI-RADS category 5) * Not pregnant or breast-feeding * Ability to lie motionless for up to 20 minutes Exclusion Criteria: * Normal Adult Volunteers * Inability to understand the risks and benefits of the study Patient Volunteers * Recent breast biopsy * Diagnostic findings from prior mammography highly suggestive of noninvasive ductal or lobular carcinoma * Uncontrolled diabetes * Diabetic and blood sugar level \> 200 mg/dL * Positive urine pregnancy test or currently breast-feeding * Inability to understand the risks and benefits of the study
References
Publications (0)
Data not yet available