Clinical trial · Interventional
Study to Assess Breast Sensation Before and After Breast Cancer Treatment
Pilot Study to Assess Breast Sensation Before and After Breast Cancer Treatment
NCT02817607CI-TRIAL-00038508withdrawnN/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 of this study is to establish techniques for evaluating breast cutaneous sensation at baseline and following either lumpectomy or mastectomy for breast cancer.
Conditions
Conditions (2)
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 Reconstruction | — | UNRESOLVED | — |
| Ductal Carcinoma In-situ | Breast Ductal Carcinoma In Situ | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Sensory testing and Biopsy | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Surgery
- interventionNames
- Procedure: Sensory testing and Biopsy
Primary outcomes (1)
- measure
- change in sensory perception score
- timeFrame
- baseline, time of surgery, 3 months, 6 months
- description
- change in sensory perception will be conducted using paired t-tests or Wilcoxon tests
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 25 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: * patients diagnosed with ductal carcinoma in-situ (DCIS) or invasive breast cancer * patients that have been offered lumpectomy or mastectomy for surgical treatment * patients with a high risk of breast cancer and are pursuing prophylactic mastectomies Exclusion Criteria: * metastatic malignancy of any kind * subjects will not have breast surgery as a portion of their breast cancer care * between 25 and 65 years old * subjects with breast implants or a history of prior breast implants * subjects that have had prior breast reduction surgery * subjects who have had radiation to one of both breasts in the past * subjects who cannot give informed consent
References
Publications (0)
Data not yet available
No reference posted for this study.