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Ductal Carcinoma In Situ clinical trials

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NCT ID: NCT05032079 Withdrawn - Clinical trials for Ductal Carcinoma in Situ

Subzero and Scorpion Trial

Start date: November 16, 2020
Phase: N/A
Study type: Interventional

This is a prospective single-institution pilot study examining the feasibility of performing ultrasound-guided cryoablation to completely ablate breast ductal carcinoma in situ (DCIS). The study is designed such that patients meeting selection criteria will undergo cryoablation followed by surgical resection. The pathology of the surgical specimen will be used to determine the rate of complete tumor ablation. Standard adjuvant therapies otherwise remained unchanged.

NCT ID: NCT04349111 Withdrawn - Clinical trials for Ductal Carcinoma In Situ

An Efficacy Study of the Xoft® Axxent® eBx® IORT System® "Lite"

Start date: June 30, 2022
Phase: N/A
Study type: Interventional

The purpose of this trial is to assess the efficacy of the Xoft Axxent eBx System when used for single-fraction IORT in early stage breast cancer. A comparison will be made to the current standard of care, whole breast irradiation (WBI), in women with early stage breast cancer.

NCT ID: NCT03437915 Withdrawn - Breast Cancer Clinical Trials

BrUOG 351: PRE-OPERATIVE APBI USING NIBB

351
Start date: March 2019
Phase: N/A
Study type: Interventional

Partial breast irradiation is typically performed after surgical removal of the tumor. Partial breast irradiation allows for focused radiation to the area from which the cancer was removed, sparing breast tissue from the potential bad effects of radiation compared to radiating the whole breast, which was the standard of care for many years. This study is evaluating the use of partial breast irradiation with NIBB performed before surgery instead of after surgery.This should allow researchers to target the cancer even more accurately and result in less normal breast tissue receiving radiation which may cause less side effects and/or a better cosmetic outcome. In this study partial breast treatment will be given with NIBB in 5 treatments over about 1 week. Surgical removal of the tumor will then be performed between 4-12 weeks following radiation treatment. Researchers believe that participant's risk of complications from surgery will not be higher after getting these radiation treatments than it would have been if participants had surgery first, but that is one of the things researchers are studying.

NCT ID: NCT02856503 Withdrawn - Breast Cancer Clinical Trials

Effect of High Dose Vitamin D on Cancer Biomarkers and Breast Cancer Tumors

Start date: January 2019
Phase: Phase 1/Phase 2
Study type: Interventional

High-doses of Vitamin D (VD) may be used as targeted therapy against breast cancer. The investigators will assess the effect of high dose VD on the following biomarkers in the breast cancer cells: VDR, estrogen receptor (ER), progesterone receptor (PR), epidermal growth factor receptor 2 (Her2/neu), androgen receptor (AR), as well as epidermal growth factor receptor 1 (EGFR) and Ki-67, as markers of proliferation, and E-cadherin, a marker of invasion and metastasis.

NCT ID: NCT02817607 Withdrawn - Clinical trials for Breast Reconstruction

Study to Assess Breast Sensation Before and After Breast Cancer Treatment

Start date: December 2016
Phase: N/A
Study type: Interventional

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.