RecruitingNot ApplicableNCT07234461

Sexual Well-being of Women Undergoing Mastectomy and Reconstruction

Sexual Well-being of Women Undergoing Mastectomy and Reconstruction: a National Survey.


Sponsor

European Institute of Oncology

Enrollment

200 participants

Start Date

Jan 21, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The study plans to collect data from patients on sexual well-being after mastectomy and immediate reconstruction by surveys. This data can support preoperative patient counselling and the prevention and care of adverse effects of cancer treatments. Specific subpopulations of mastectomy women showing severe sexual impairment can be outlined; they may benefit from lifestyle changes and intervention strategies (intravaginal use of diazepam, local hyaluronic acid, intravaginal use of spermidine, pelvic floor gymnastic and physiotherapy). Our goal is to improve quality of life of breast cancer patients.


Eligibility

Sex: FEMALEMin Age: 18 Years

Inclusion Criteria5

  • Patients undergoing mastectomy for primary breast cancer;
  • High-risk healthy patients undergoing risk reducing mastectomies;
  • Unilateral and/or bilateral mastectomies;
  • If unilateral mastectomy, both patients requiring or not contralateral mammaplasty of the healthy breast;
  • All reconstructive procedures included (autologous and heterologous reconstructions).

Exclusion Criteria4

  • Patients undergoing breast conservation;
  • Patients who previously underwent breast cancer treatment, requiring further surgery for local relapse or secondary breast cancers;
  • Delayed post-mastectomy reconstructions;
  • Patients not available for e-correspondence.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERSurvey using a questionnaire.

Questionnaires collecting sociodemographic information and their sexual well-being.


Locations(19)

Azienda Ospedaliero Universitaria Consorziale Policlinico

Bari, Italy, Italy

Istituto Tumori Giovanni Paolo II

Bari, Italy, Italy

Policlinico Sant'Orsola-Malpighi

Bologna, Italy, Italy

Ospedale Bufalini di Cesena

Cesena, Italy, Italy

Presidio Ospedaliero GB Morgagni-Pierantoni

Forlì, Italy, Italy

European Institute of Oncology

Milan, Italy, Italy

Ospedale Mater Olbia

Olbia, Italy, Italy

Azienda Ospedale Università di Padova

Padova, Italy, Italy

Policlinico Paolo Giaccone

Palermo, Italy, Italy

Policlinico San Matteo

Pavia, Italy, Italy

Azienda Ospedaliero Universitaria Pisana

Pisa, Italy, Italy

Campus Biomedico

Roma, Italy, Italy

Istituto Tumori Regina Elena

Roma, Italy, Italy

Policlinico Gemelli

Roma, Italy, Italy

A.O.U. Città della salute e della scienza di Torino

Torino, Italy, Italy

Azienda Ospedaliera di Treviso

Treviso, Italy, Italy

Ospedale di Cattinara

Trieste, Italy, Italy

Ospedale Universitario di Udine

Udine, Italy, Italy

Breast Unit Settelaghi

Varese, Italy, Italy

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07234461


Related Trials