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Mastectomy clinical trials

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NCT ID: NCT05395936 Terminated - Breast Cancer Clinical Trials

Mastectomy Flap Temperature Study

Start date: September 29, 2022
Phase: N/A
Study type: Interventional

The purpose of this research study is to measure tissue temperatures and generate a prospective database of participants undergoing mastectomy with or without breast reconstruction at Wake Forest Baptist Hospital (WFBH) in order to enable and facilitate the evaluation of important and novel research questions - and quality improvement (QI) ideas/objectives - that may improve the care of breast surgery patients.

NCT ID: NCT05126615 Terminated - Mastectomy Clinical Trials

Contribution of Auriculotherapy in the Management of Mastectomy With Immediate Reconstruction by Latissimus Dorsi Flap (ATMAGD)

ATMAGD
Start date: May 10, 2019
Phase: N/A
Study type: Interventional

Over the past decade, more and more healthcare professionals are using auriculotherapy as a preventative and effective therapy for pain. This therapy is applied by odontologists, anesthetists, surgeons, etc., to alleviate chronic pain. The effects of auriculotherapy are known in particular in reducing preoperative anxiety, pain in cancer patients and postoperative pain. The aim of this study is to assess the effectiveness of adding auriculotherapy to the standard global anesthetic protocol, compared to this single reference protocol, on the incidence at 3 months post-intervention of Chronic Post-Surgical Pain, in patients operated for a mastectomy with reconstruction immediate by latissimus dorsi flap.

NCT ID: NCT00943605 Terminated - Mastectomy Clinical Trials

PEAK PlasmaBladeā„¢ 4.0 Versus Traditional Electrosurgery in Mastectomy

PRECISE
Start date: June 2009
Phase: N/A
Study type: Interventional

The objective of this clinical study is to evaluate the incidence of partial skin necrosis following modified-radical mastectomy with or without same-day (two-stage) reconstruction with the PEAK PlasmaBlade 4.0; to monitor and record operative performance, post-operative pain, drain output, and skin scarring following surgery; and to compare these endpoints to the current standard of care (SOC).

NCT ID: NCT00616824 Terminated - Postoperative Pain Clinical Trials

The Use of an Acellular Dermal Matrix in a Two-Staged Breast Reconstruction

Start date: September 2007
Phase: Phase 4
Study type: Interventional

This study intends to compare postoperative outcomes of a tissue expander placement following a mastectomy with two different operative techniques. This study will be randomized and double blinded comparing the traditional placement of the tissue expander under an inferolateral serratus muscle flap to a new technique which uses an acellular dermal matrix as an inferolateral sling, instead of the muscle flap. The study we are proposing will evaluate the question of whether there is a difference between the traditional method of serratus flap and the new technique of using an acellular matrix with tissue expander placement. This will be a double blinded randomized study of thirty women in each group comparing outcomes which will include postoperative pain, complications (wound infection, hematoma, capsular contracture, etc), and patient satisfaction with the procedure.