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Spots Global Cancer Trial Database for Therapeutic Nipple Sparing Mastectomy.

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Trial Identification

Brief Title: Therapeutic Nipple Sparing Mastectomy.

Official Title: Therapeutic Nipple Areola Skin-sparing Mastectomy.

Study ID: NCT02311959

Conditions

Breast Cancer

Study Description

Brief Summary: This is a phase III, multicentric, single arm study with a sequential design using the exact conditional Poisson test. The primary objective of this prospective study is to evaluate whether selected breast carcinoma patients could be treated with nipple sparing mastectomy (NSM) with an acceptable low local recurrence rates. 450 patients will be included over a period of 4 years and will be followed for a 5 years period (twice a year). All patients must have a complete preoperative evaluation (bilateral mammography, bilateral breast ultrasonography +/- MRI), and a histopathological diagnostic proof of carcinoma (invasive or in situ, all histopathological types, first treatment or relapse). The study procedure is represented by nipple areola skin-sparing mastectomy followed by immediate breast reconstruction. After surgery, early and late complications, including specific complications (suffering of the nipple-areolar complexe and suffering of the skin flaps), will be evaluate. An esthetic evaluation (by patient and clinician) and a quality of life evaluation will be realized throughout the study. A complementary study, prospective, non-interventional, will be proposed to patients who will benefit from the same surgical technique (NSM) followed by immediate reconstruction, but in the context of preventive surgery (prophylactic surgery for patients mutated or high genetic risk). The aim of this complementary study, which will include a maximum of 60 patients, is to evaluate associated morbidity in prophylactic NSM. Data will be collected over a 3 months period after surgery.

Detailed Description:

Eligibility

Minimum Age: 40 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Centre Hospitalier de Blois, Blois, , France

Institut Bergonie, Bordeaux, , France

Pôle santé Léonard de Vinci, Chambray-lès-Tours, , France

Centre Georges Francois Leclerc, Dijon, , France

Hôpital privé Drôme Ardèche, Guilherand-Granges, , France

Clinique du Mail, La Rochelle, , France

Centre Hospitalier Universitaire Grenoble Alpes, La Tronche, , France

Clinique Saint Amé, Lambres-lez-Douai, , France

Hopital de Levallois-Perret, Levallois-perret, , France

Centre Oscar Lambret, Lille, , France

Centre Leon Berard, Lyon, , France

Hôpital de la Croix Rousse, Lyon, , France

Institut Paoli Calmettes, Marseille, , France

Clinique Clementville, Montpellier, , France

Centre Hospitalier Universitaire de Montpellier, Montpellier, , France

Institut Du Cancer de Montpellier, Montpellier, , France

Centre Antoine LACASSAGNE, Nice, , France

Hôpital Européen Georges Pompidou, Assistance Publique - Hôpitaux de Paris, Paris, , France

Ap-Hp - Hopital Tenon, Paris, , France

CHRU Lyon Sud, Pierre Benite, , France

Centre Hospitalier de Poitiers, Poitiers, , France

Centre Eugène Marquis, Rennes, , France

Centre Henri Becquerel, Rouen, , France

Clinique Mathilde, Rouen, , France

Hôpital René Huguenin, Saint-cloud, , France

Clinique Mutualiste Chirurgicale, Saint-Etienne, , France

Etablissement Rennais du Sein - CHP St Grégoire, Saint-Grégoire, , France

INSTITUT DE CANCEROLOGIE DE L'OUEST - Site René Gauducheau, Saint-Herblain, , France

Hôpital Privé de la Loire, Saint-Étienne, , France

Institut Claudius Regaud, Toulouse, , France

Clinique Saint Jean, Toulouse, , France

Institut de Cancerologie de Lorraine, Vandoeuvre-Les-Nancy, , France

Institut Gustave Roussy, Villejuif, , France

Contact Details

Name: Eva JOUVE, Md.

Affiliation: IUCT-O

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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