Clinical trial · Observational
Anatomical Landmarks for Chest Wall Perforators Used for Partial Breast Reconstruction
Anatomical Landmarks for Chest Wall Perforators Used for Partial Breast Reconstruction (LaPBrecon)
NCT07006662CI-TRIAL-00114087(LaPBrecon)recruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 10, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260910-000001
Summary
Brief summary (as posted)
The aim of this 6-month proof-of-concept study is to map out the chest wall perforators in relation to anatomical landmarks for partial breast reconstruction.
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 Female | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (4)
- measure
- Location of vesselse
- timeFrame
- 6 months
- description
- The location of the AICAP vessels in vertical and horizontal axis using constant bony and soft tissue landmarks. This will be measured by the distance of the perforators from the anatomical landmarks
- measure
- Location of vessels
- timeFrame
- 6 months
- description
- The location of the MICAP vessels in vertical and horizontal axis using constant bony and soft tissue landmarks. This will be measured by the distance of the perforators from the anatomical landmarks
- measure
- Location of vessels
- timeFrame
- 6 months
- description
- The location of the LTAP vessels in vertical and horizontal axis using constant bony and soft tissue landmarks. This will be measured by the distance of the perforators from the anatomical landmarks
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients undergoing elective breast surgery * Age ≥ 18 years * Female * BMI ≤ 30 kg/m2 * Willing and able to give fully informed consent, * Willing and able to comply with the study procedures Exclusion Criteria: * Pregnant patients * Previous bilateral Breast or axillary surgery * Undergoing bilateral oncoplastic procedure or requiring bilateral pre-operative marking * Undergoing breast surgery requiring pre-operative marking of some of the landmarks and has had contralateral breast or axillary surgery in the past * Surgery planned within 24 hours of screening for eligibility * Known history of allergy or contact dermatitis to ultrasound gels
References
Publications (0)
Data not yet available
No reference posted for this study.