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Clinical Trial Summary

Primary objectives: - To estimate Sexual Dysfunction (SD) incidence in premenopausal breast cancer patients treated by surgery and taking endocrine therapy. - To detect the presence of SD-related distress in the population, as a determining factor in the maintenance of a good quality of life. Secondary objectives: - To describe SD characteristics determining the most frequently reported symptoms and correlations with type of surgery or therapeutic regimens. - Collect baseline data for subsequent randomized trials involving practical interventions with the aim to reduce SD prevalence in this population.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06458764
Study type Observational [Patient Registry]
Source Candiolo Cancer Institute - IRCCS
Contact
Status Recruiting
Phase
Start date May 1, 2023
Completion date March 1, 2025

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