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Clinical trial

Efficacy, Safety, Cosmesis and Patient Satisfaction With Vacuum-Assisted Percutaneous Excision (VAPE) Compared With Standard Surgical Excision (X) of Non-malignant, Borderline or High-risk Breast Lesions: A Randomized Controlled Trial

NCT03868475 is registered in ClinicalTrials.gov with London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's as lead sponsor.

NCT NCT03868475
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Registry record

As filed in ClinicalTrials.gov.

Title
Efficacy, Safety, Cosmesis and Patient Satisfaction With Vacuum-Assisted Percutaneous Excision (VAPE) Compared With Standard Surgical Excision (X) of Non-malignant, Borderline or High-risk Breast Lesions: A Randomized Controlled Trial
Lead sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Phase
Not applicable
Overall status
Withdrawn
Start date
January 31, 2025
Completion date
January 1, 2028
Enrollment
0 (actual)
Sites
Not reported

Conditions

As the registry lists them; a condition with its own page is linked.

atypical ductal hyperplasia, atypical lobular hyperplasia, breast fibroadenoma, breast papilloma, complex sclerosing papillary lesion of the breast, flat epithelial atypia, lobular carcinoma in situ, phyllodes breast tumor, phyllodes; fibroadenoma, radial scar