Skip to content

Monitoring bone defects of the femur before hip revision and bone growth after hip revision arthroplasty with DEXA, a pilot study

Monitoring bone defects of the femur before hip revision and bone growth after hip revision arthroplasty with DEXA, a pilot study - DEXA and hip revision arthroplasty, a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON39308
Enrollment
25
Registered
2011-05-30
Start date
2012-11-06
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

hip revision arthroplasty

Interventions

None listed

Sponsors

Reinier de Graaf Groep
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: The hospital criteria and protocol for patients who are diagnosed for a total hip revision will be applied. - Diminished femoral bone stock - patients needing revision surgery - Patient aged 18y and older - Patient willing to participate - No active infection - ASA I-III

Exclusion criteria

Exclusion criteria: - Patients unwilling to participate - Mentally retarded - Patients with sufficient bone stock - ASA IV / V

Design outcomes

Primary

MeasureTime frame
Main study parameters are bone mineral density and bone mineral content. It is expected that these DEXA results of the revised hip after 24 months will be comparable to DEXA results of the contralateral hip. Bone mineral density and bone mineral content will increase in time when DEXA scans after surgery are compared.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)