Clinical Trials Directory

Trials / Terminated

TerminatedNCT01623908

Bone Loss Treatment From Adjuvant Zoledronate Efficacy

An Open,Multicentre,Prospective Study of Adjuvant Zoledronate Treatment in Osteoporosis Women With Breast Cancer

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
First Affiliated Hospital, Sun Yat-Sen University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The main purpose of this study is to observe and assess the impact of adjuvant zoledronate on bone density in breast cancer patients. The second purposes: * The efficacy of adjuvant zoledronate * The safety of adjuvant zoledronate * The bone loss of breast cancer patients in Guangdong * The correlation between bone loss of breast cancer patients and treatment of disease in Guangdong

Detailed description

Breast cancer is the most commonly diagnosed malignant disease and the leading cause of cancer-related mortality among women. Zoledronate is a bone-targeted bisphosphonate, which is used to treat osteoporosis and to reduce the risk of skeletal morbidity in patients with bone metastases. Zoledronate can also reduce the persistence of disseminated tumour cells in the bone marrow of women with early-stage breast cancer. Nowadays, consensus is emerging that certain subsets of patients with early-stage breast cancer may benefit from bisphosphonate therapy.

Conditions

Interventions

TypeNameDescription
DRUGZoledronate4mg, IV (in the vein) every 6 months. Number of Cycles: up to the researcher or until unacceptable toxicity develops.

Timeline

Start date
2011-07-01
Primary completion
2013-06-01
Completion
2013-06-01
First posted
2012-06-20
Last updated
2021-06-22

Locations

10 sites across 1 country: China

Source: ClinicalTrials.gov record NCT01623908. Inclusion in this directory is not an endorsement.