Zoledronic Acid With Intermittent Hormonal Therapy in Patients With Prostate Cancer
NCT ID: NCT00226954
Last Updated: 2020-03-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
PHASE2
23 participants
INTERVENTIONAL
2003-03-31
2009-02-28
Brief Summary
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To determine the duration of use of zoledronic acid in improving Bone mineral density in patients with prostate cancer who are on hormones intermittently.
Secondary Objectives:
To describe the safety and tolerability at this dose and schedule
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Zoledronic Acid with Intermittent Hormonal Therapy
zoledronic acid
Interventions
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zoledronic acid
Eligibility Criteria
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Inclusion Criteria
18 Years
MALE
No
Sponsors
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Novartis
INDUSTRY
Stanford University
OTHER
Responsible Party
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Sandy Srinivas
PI
Principal Investigators
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Dr. Sandy Srinivas
Role: PRINCIPAL_INVESTIGATOR
Stanford University
Locations
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Stanford University School of Medicine
Stanford, California, United States
Countries
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Other Identifiers
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78869
Identifier Type: -
Identifier Source: secondary_id
NCT00226954
Identifier Type: -
Identifier Source: secondary_id
PROS0001
Identifier Type: -
Identifier Source: secondary_id
PROS0001
Identifier Type: -
Identifier Source: org_study_id
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