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Research for markers of bone quality

Research for markers of bone quality - CLAST study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31945
Enrollment
100
Registered
2007-12-18
Start date
2008-08-04
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Osteoporosis

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Postmenopausal women with a vertebral fracture and postmenopausal women without a vertebral fracture with high bone mineral density (T-score >-1 S.D.)

Exclusion criteria

Exclusion criteria: Medication influencing osteoclast function and formation (Bisphosphonates, Hormone Replacement Therapy, Strontium Ranelate, Teriparatide, Raloxifen)

Design outcomes

Primary

MeasureTime frame
Osteoclast formation will be studied by staining them with a Tartrate Resistant Acid Phosphatase staining. Bone resorption will be studied using a pit-assay to determine the surface and the number of resorption pits.

Secondary

MeasureTime frame
To study the expression of genetic markers of bone resorption and fractures, osteoclast will be seeded for RNA isolation. Furthermore, since osteoclast are derived from the hematopoietic line like lymfocytes, the PBMCs will be used to study the influence of lymfocytes and factors derived from lymfocytes on osteoclasts. Furhtermore blood will be collected as well to study biochemic and serum markers to be able to relate them to osteoporosis or other pathology.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)