Clinical Trials Directory

Trials / Completed

CompletedNCT02440230

Safety of OFS Combined With AI Endocrine Therapy in Chinese Premenopausal Breast Cancer Patients

Safety of Ovarian Function Suppression(OFS)Combined With Different Aromatase Inhibitors(AIs) Endocrine Therapy in Chinese Premenopausal Breast Cancer Patients:A Randomized, Controlled, Prospective, Observational Study

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
110 (actual)
Sponsor
Shanghai Jiao Tong University School of Medicine · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

To compare safety of adjuvant OFS combined with anastrozole versus OFS combined with exemestane in Chinese premenopausal hormonal receptor(HR) positive breast cancer patients.

Conditions

Interventions

TypeNameDescription
DRUGOFS + AnastrozoleOvarian function suppression can be achieved by choice of goserelin at a dose of 3.6 mg administered by means of subcutaneous injection every 28 days,bilateral oophorectomy,or bilateral ovarian irradiation. Patients will take anastrozole 1mg qd.
DRUGOFS + ExemestanePatients will take exemestane 25mg qd. Ovarian function suppression can be achieved by choice of goserelin at a dose of 3.6 mg administered by means of subcutaneous injection every 28 days,bilateral oophorectomy,or bilateral ovarian irradiation.

Timeline

Start date
2015-05-01
Primary completion
2021-12-01
Completion
2021-12-01
First posted
2015-05-12
Last updated
2022-12-30

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02440230. Inclusion in this directory is not an endorsement.