Clinical trial · Observational
Sensory Morbidity Following Breast Surgery
NCT00625924CI-TRIAL-00013476completedClinicalTrials.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 goal of the study is measure breast sensations after breast surgery. The results of this study will help surgeons better understand breast sensations and may improve the way surgery is done.
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 |
|---|---|---|---|
| questionnaires | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- label
- 1
- description
- autogenous tissue breast reconstruction
- interventionNames
- Behavioral: questionnaires
- label
- 2
- description
- tissue expander/implant breast reconstruction
- interventionNames
- Behavioral: questionnaires
- label
- 3
- description
- mastectomy alone
- interventionNames
- Behavioral: questionnaires
Primary outcomes (1)
- measure
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 21 Years
Show eligibility criteria text
Inclusion Criteria: * The Samples used will be derived from three cohorts below and will only include patients who have completed mastectomy or reconstruction within 1-5 years of enrollment. * Patients who have undergone immediate, two-stage expander/implant postmastectomy reconstruction * Patients who have undergone immediate, autogenous tissue flap reconstruction following mastectomy * Patients who have undergone mastectomy alone * Patients at least 21 years of age * Patients who completed mastectomy ± immediate post-mastectomy reconstruction at least one year but no longer than five years prior to study entry Exclusion Criteria: * Patients who have had any of the following: * delayed reconstruction (no reconstruction at time of surgery) combined autogenous tissue/implant breast reconstruction, and/or * Patients who have a pre-surgical history of complex regional pain syndrome * Patients who have had radiation therapy * Patients who have had a local recurrence * Patients who do not speak the English language (validated translations of key questionnaires are not available).
References
Publications (0)
Data not yet available
No reference posted for this study.