A Multicentre Prospective Study to Investigate the Prevalence of Sexual Dysfunction and Quality of Life in Women with Breast Cancer receiving Aromatase Inhibitors (ACTRN12607000068460)
A Multicentre Prospective Study to Investigate the Prevalence of Sexual Dysfunction and Quality of Life in Women with Breast Cancer receiving Aromatase Inhibitors
Beobachtungsstudie
Phase nicht angegeben
Investigative Site
Sponsor: Professor Michael Friedlander
Zuletzt aktualisiert: 21. Januar 2007 Hinweis - Die Informationen stammen aus öffentlichen Registern und spiegeln möglicherweise nicht die Echtzeitänderungen am lokalen Studienzentrum wider.
Whilst the long-term effects of chemotherapy and hormonal therapy with tamoxifen on sexual function and quality of life of women with breast cancer has been well documented, less is known about the impact of aromatase inhibitors (AIs) on a woman’s sexual functioning. Common sexual issues raised have included vaginal dryness, painful sexual intercourse (dyspareunia) and a reduction in libido. AIs have largely replaced tamoxifen as choice of hormonal treatment in post-menopausal women and as there will an increasing number of women on AIs, it is important to document the impact of AI use on sexual functioning. The result of this study will raise the awareness of the potential effects of AI use and sexual dysfunction for both the physician and patient.
Primary breast cancer. Post-menopausal (no menstrual periods for at least 6 months). 6-8 weeks post chemotherapy Not receiving adjuvant anti-oestrogen therapy at time of study entry Fluent in English Willingness to complete questionnaire.
Ausschlusskriterien
Diagnosis of metastatic breast cancer.
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Design-Details
ZuteilungN/A
InterventionsmodellN/A
MaskierungN/A
Anzahl der Teilnehmer200
Arme & Interventionen
Arme
Interventionen
Keine Interventionen verfügbar.
Ergebnismessungen
Primäre Ergebnismessungen
At baseline and at 3 and 6 months after commencing on aromatase inhibitors.
Sexual activity questionnaire
Sekundäre Ergebnismessungen
Dyspareunia – visual analog scaleAt baseline and at 3 and 6 months after commencing on aromatase inhibitors.
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