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Spots Global Cancer Trial Database for Efficacy Study of Single Stage Breast Reconstruction in Female Participants With Mastectomy

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Trial Identification

Brief Title: Efficacy Study of Single Stage Breast Reconstruction in Female Participants With Mastectomy

Official Title: A Prospective, Multicenter, Controlled Study of Implant-based Breast Reconstruction, Measuring the Safety, Efficacy and Outcomes, of Immediate Single Stage Breast Reconstruction With Stratticeā„¢ Reconstructive Tissue Matrix Versus Immediate Two Stage Breast Reconstruction Without Stratticeā„¢ TM (ESSBR-Efficacy of Single Stage Breast Reconstruction)

Study ID: NCT01910298

Study Description

Brief Summary: The purpose of this study was to compare the efficacy of immediate single-stage post-mastectomy breast reconstruction with Strattice Reconstructive Tissue Matrix (Strattice) as compared to immediate two-stage post-mastectomy breast reconstruction where the initially placed expander was exchanged for a breast implant only, without any type of reinforcement.

Detailed Description: The primary objective of this study is to compare the efficacy of immediate single-stage post-mastectomy breast reconstruction with Stratticeā„¢ TM, otherwise referred to as DTI as compared to immediate two-stage post-mastectomy breast reconstruction where the initially placed expander will be exchanged for a breast implant only, without any type of a reinforcement. The objective will be achieved by prospectively assessing the number of planned and unplanned post-mastectomy surgical interventions within 12 months of the mastectomy. Two-stage breast reconstruction will include the initial placement of a tissue expander in a total or partial submuscular position. In the case of partial muscle coverage, this will be without the support of any mesh or autologous flap to reinforce the lower pole. The expander will be inflated over approximately the next one to six months, and then replaced with an implant.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Institut Bergonie, Bordeaux, , France

Centre Oscar Lambret, Lille Cedex, , France

Institut du Cancer de Montpellier Val d'Aurelle, Montpellier Cedex 5, , France

L'Institut du Sein- Paris Breast Center, Paris, , France

Hopital Tenon APHP, Paris, , France

UniversitƤtsklinikum Erlangen, Erlangen, , Germany

Kliniken Essen-Mitte, Essen, , Germany

UniversitƤtsklinikum Freiburg, Freiburg, , Germany

Medizinische Hochschule Hannover, Hannover, , Germany

UniversitƤts-Frauenklinik Heidelberg, Heidelberg, , Germany

Klinik der UniversitƤt MĆ¼nchen, Campus Innenstadt, Munich, , Germany

Klinikum rechts der Isar, Munich, , Germany

Asklepios Paulinen Klinik, Wiesbaden, , Germany

St Luke's hospital / Bradford Royal Infirmary (BRI), Bradford, , United Kingdom

Dorset County Hospital, Dorchester, , United Kingdom

Frimley Park Hospital, Frimley, , United Kingdom

Wythenshawe Hospital UHSM NHS Foundation Trust, Manchester, , United Kingdom

City Hospital, Nottingham, , United Kingdom

Contact Details

Name: Donna Jacobs

Affiliation: Allergan

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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