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Bone density measurement methods during androgen deprivation

BONE MINERAL DENSITY IN PROSTATE CANCER PATIENTS TREATED WITH ANDROGEN DEPRIVATION THERAPY

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON22104
Enrollment
51
Registered
2013-06-24
Start date
2013-06-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Prostate cancer, andogen deprivation, bone density Prostaatkanker, androgeen deprivatie, botdichtheid

Interventions

By measuring BMD by two different methods, the change in BMD estimated bye ach method will be compared

Sponsors

SFG, Rotterdam, The Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age >18 years 1. Indication for ADT as treatment for nonmetastatic prostate cancer according to the Bolla schedule; 2. Planned ADT or recently started ADT (max 4 weeks before baseline DEXA measurement); 3. Signed informed consent.

Exclusion criteria

Exclusion criteria: Pre-existing indication for osteoporosis treatment, i.e. before the baseline DEXA scan. 1. Current or prior treatment with bisphosphonates and/or RANK ligand inhibitors.

Design outcomes

Primary

MeasureTime frame
Agreement between the change in Achilles T-scores and the change in DEXA scan T-scores.

Secondary

MeasureTime frame
Association of repeated delta T-scores over time of the DEXA and Achilles scans • Association between (absolute) Achilles T-scores and (absolute) DEXA T-scores at each available time point.

Contacts

Public ContactA.P. Hamberg

PO Box 5201

p.hamberg@sfg.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)