Skip to content

Bone Loss in Men on Androgen Blockade as Adjuvant Therapy for Prostate Cancer

Bone Loss in Men on Androgen Blockade as Adjuvant Therapy for Prostate Cancer

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00199537
Enrollment
25
Registered
2005-09-20
Start date
2005-02-28
Completion date
2008-02-29
Last updated
2008-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone Loss, Prostate Cancer

Brief summary

Patients with advanced prostate cancer undergoing adjuvant treatment with androgen blockade will be followed over a 1 year interval to assess the effects of this treatment on bone metabolism. It is expected that men undergoing androgen blockade will experience accelerated bone loss.

Interventions

None listed

Sponsors

Lawson Health Research Institute Internal Review Fund
CollaboratorUNKNOWN
University of Western Ontario, Canada
CollaboratorOTHER
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Men * Age of 40 years or greater * Diagnosis of advanced prostate cancer (ie: prostate-specific antigen \[PSA\] less than 25 ug/L and undergoing continued treatment with leuteinizing hormone-releasing hormone \[LHRH\] therapy) * Willing and able to consent

Exclusion criteria

* Metastatic disease to bone * Medications affecting bone turnover (bisphosphonate, steroids, anticonvulsant) * Renal failure (serum creatinine \> 200 umol/L) * Co-morbidity factors affecting bone density (ie: Paget's, rheumatoid arthritis) * Factors affecting ability to perform the bone density tests using femoral head measurements (ie: bilateral hip arthroplasty) * Cancer other than skin, except when, in the investigators' opinion, it is determined to be appropriate and not adversely affect the outcome of the trial * Gastrointestinal (GI) pathology (eg. malabsorption syndrome) * Parathyroid disease

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026