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Periprosthetic bone mineral density (BMD) around two different stems in total hip arthroplasty

Periprosthetic bone mineral density (BMD) around two different stems in total hip arthroplasty: an observational longitudinal study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN54967983
Enrollment
50
Registered
2010-08-18
Start date
2008-06-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Osteoarthritis of the hip Musculoskeletal Diseases Osteoarthritis

Interventions

In all patients the Metha short stem (monoblock with 130° CCD angle and 0° ante-, retrotorsion) or the Bicontact stem (AESCULAP AG, Tuttlingen, Germany) was implanted by three experienced senior surge

Sponsors

German Research Council (Deutsche Forschungsgemeinschaft [DFG]) (Germany)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Indication for unilateral implantation of the Bicontact stem or the Metha short stem due to osteoarthritis of the hip 2. Patients' ages between 35 and 70 years of either sex 3. Written informed consent

Exclusion criteria

Exclusion criteria: 1. Manifestly overweight (body mass index [BMI] greater than 35 kg/m^2) 2. History of previous surgeries on the same hip 3. Femoral fractures 4. Metabolic bone diseases 5. Use of steroids or other drugs affecting bone metabolism 6. Intraoperative cracks 7. Severe osteoarthritis of the contralateral hip 8. Received total hip arthroplasty (THA) on the contralateral hip during the study period 9. Patients in whom an event leading to restricted weight bearing on the ipsi- or contralateral hip occurred

Design outcomes

Primary

MeasureTime frame
BMD (g/cm^2) in Gruen Zones 1 - 7 per DEXA, measured 1 day pre-operatively, and 1 week, 6 months, 1 year, 2 years, 3 years and 4 years post-operatively.

Secondary

MeasureTime frame
Harris Hip Score per questionaire and clinical examination, measured 1 day pre-operatively, and 1 week, 6 months, 1 year, 2 years, 3 years and 4 years post-operatively.

Countries

Germany

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026